Implant Brands
Which country are DIO implants from?
South Korea, Busan; founded in 1988, moved into implants in 2002. As of 2024 its largest shareholder is a company set up by a Korean investment fund
You will mostly come across the DIO name as 'DIOnavi' or 'UF II': one is a digital guided surgery system, the other an implant line. The answer to the country question is short. The information that will be useful to you years from now, though, is which line went into your mouth, in which size, and whether you were given this in writing.
Short answer
DIO is a South Korean brand: DIO Corporation was founded in 1988, its head office is in Busan and it has been traded on Korea's KOSDAQ exchange since 2000. It began manufacturing dental implants in 2002. Its largest shareholder is DIO Holdings, set up in 2018 by NICE Investment Partners, part of Korea's NICE group; in 2024 a fund called H PE also joined the management. Its well-known lines are UF(II), UFIII, UNICON, SICON, FTN and Protem; DIOnavi is the company's guided surgery system.
- Country of origin
- South Korea, Busan; 1988
- Implant manufacturing
- Since 2002
- Largest shareholder
- DIO Holdings (NICE Investment Partners)
- Well-known lines
- UF(II), UFIII, UNICON, SICON, FTN, Protem; DIOnavi
Who DIO is, and who owns it
According to the company's own history, DIO was founded in South Korea in 1988. It was a medical device manufacturer before it moved into implants too: it received the European CE certificate in 1995 and the ISO 9001 quality certificate in 1997. In 2000 it was listed on KOSDAQ, Korea's technology exchange. It started in the dental implant business in 2002. In other words, the company's age and its implant history are not the same: on the implant side, we are talking about a history of roughly twenty-four years. Its history also includes non-dental products such as coronary stents.
The head office is in Busan. In submissions to the FDA, the US food and drug agency, the manufacturer's address is given as the Haeundae district of Busan. In 2020 the company opened a research centre in the Magok district of Seoul. On the production side, however, there is no single address: the history states that a production company was set up in China in 2017 and that the DIO VINA company in Vietnam was acquired in 2020. That is why where a DIO product that reaches you was made is told not by a general statement but by the label on its box.
Ownership has changed hands, or come close to doing so, several times. NICE Investment Partners, a private equity fund belonging to Korea's NICE group, set up a company called DIO Holdings for this investment in 2018; according to the Korean press, in 2024 DIO Holdings was the largest shareholder with 21.1 per cent of the company. In March 2022 an agreement was signed for the sale of DIO to Sesim, a company owned by Hong Sung-bum, the founder of the botulinum toxin manufacturer Hugel; but the agreement was cancelled the same year when the buyer withdrew.
In 2024 a Korean fund called H PE invested in the company in exchange for convertible bonds, according to the Korean press, and joined the management alongside NICE. In short, DIO is in Korea in both its origin and its ownership; it is not a brand that has come under the roof of a foreign group, as Neodent or Alpha-Bio have.
DIO is not a single implant but a family. The company's current product list includes the UF(II), UFIII, UNICON, SICON and FTN lines and the one-piece Protem implant. UF first came out in 2011; UF(II) is the next generation of this line. According to the summary document submitted to the FDA, UF(II) is made of grade 4 pure titanium and its surface is roughened by sandblasting and acid; it is produced in diameters from 3.8 to 5.5 mm and lengths from 7 to 16 mm. UFIII came onto the market in 2023, UNICON in 2025 and SICON in 2026.
What sets DIO apart from the other Korean brands is its digital side. DIOnavi was introduced in 2014: a CBCT scan and an intraoral scan are combined and the position of the implant is planned on a computer, then the implant is placed with a surgical guide produced according to this plan. In 2018 DIOnavi Full Arch was added for fully edentulous jaws. In its own history the company writes that 17,000 jaws worldwide have been reached with DIOnavi Full Arch; this figure is the manufacturer's own statement.
How accurate guided surgery is, on the other hand, is a matter that has been measured independently of the manufacturer. In a 2018 meta-analysis combining 20 clinical studies, the mean deviation from the planned position of implants placed with a static surgical guide was found to be 1.2 mm at the entry point, 1.4 mm at the tip and 3.5 degrees in angle; the deviation was greater in fully edentulous jaws than in partially edentulous ones. The authors recommend leaving a safety margin of at least 2 mm. In other words, a guide reduces the error, but does not bring it to zero.
The factual answer to 'is it any good': it is a system from a company that has been producing implants for more than twenty years, many of whose products have been put on the market in the USA through the FDA 510(k) route, and which is mentioned in independent publications. But published long-term patient follow-up carrying the DIO name is scarce compared with that of the big brands; a significant part of the publications are laboratory studies or small clinical studies. The outcome, meanwhile, is determined by planning, how the load is spread, smoking and diabetes control and regular maintenance more than by the brand name. The implant used in our protocol of fixed teeth in 72 hours with the Ihde method belongs to a different class: a one-piece corticobasal implant that anchors in the hard outer layer of the jaw.
When a conventional system like DIO is a sensible choice
The points below are not specific to DIO alone; they look at the two-piece implant design that sits inside the bone and usually needs healing time, and at guided surgery.
When it fits
- If the CBCT scan shows enough boneA conventional implant needs width and height in the inner part of the bone. If the volume is there, it can be placed without any additional procedure; for narrow areas DIO also has slim-bodied options.
- If immediate loading will be based on measurementAccording to the document submitted to the FDA, UF(II) can be loaded immediately only when good initial anchorage is achieved and the bite load is adjusted appropriately. If this measurement is going to be taken and put on record, the plan is transparent.
- If guided surgery has really been plannedWith a system like DIOnavi, the CBCT scan, the intraoral scan and the digital plan are done in advance. Being shown the plan on screen and having the implant's distance from the nerve or the sinus explained to you shows that the guide is doing its job.
- If you already have DIO in your mouthContinuing with the same line keeps your inventory of parts simple. But first it has to be known for certain whether the existing implant is UF(II), FTN or another line.
When it doesn't
- If there is advanced bone resorptionIf there is no volume left to anchor in, a conventional implant often needs a graft or a sinus procedure first, and treatment stretches over months. In this situation, a different class of implant that uses the hard outer layer of the bone should also be discussed.
- If you are told 'it is guided, so it is error-free'Independent measurements show that there is deviation at the millimetre level with a guide too. A guide does not make safe a plan that was made without leaving a safety margin.
- If you are not given the line and size details'A Korean implant' or 'we fitted DIO' is not a record. If the line name, diameter, length and lot number are not written down, the dentist who works in that mouth later on will be guessing when choosing parts.
- If price is the only reason for the choicePrice is a legitimate criterion, but on its own it says nothing about whether the implant suits your mouth. Suitability is read from a CBCT scan and an examination.
Five questions to ask when DIO is recommended
They are short questions. If the answers are clear, there is a considered choice behind the plan; every answer that stays vague is a gap you will have to fill in later.
- 1
Which line will be used?
UF(II), UFIII, UNICON, SICON, FTN or Protem. It should be possible to explain the choice in terms of the density, width and height of your bone.
- 2
If DIOnavi is going to be used, can I see the plan?
In guided surgery the position of the implant is determined on a computer before the procedure. Asking for a screenshot of the plan and for the distance between the implant and the nerve or the sinus is a normal request.
- 3
If there is immediate loading, will the anchorage be measured?
Fitting teeth on the same day is a decision made when sufficient anchorage is measured during placement. You can ask for the measured value to be written into your record.
- 4
Can I see the barcode on the label?
Medical devices put on the market in Turkey must be registered in the Product Tracking System (ÜTS). The number on the label shows the product's manufacturer and its registration; the place of manufacture, too, is most often told by the label.
- 5
Where do parts come from, and how long do they take?
According to the company's history, DIO set up a company in Turkey in 2020. Ask whether the clinic has stock and, if not, how long it takes to obtain a screw and a top part.
Things that make more difference than the name of the line
If the first four points below are in place, the difference between brands narrows; if they are not, no brand makes up for the gap.
A complete record
Line name, connection type, diameter, length, lot number and the area where it was placed. If you have this information, another dentist can pick up the work where it was left off.
A plan that leaves a safety margin
Guided or not, the implant's distance from the nerve, the sinus and the neighbouring root is planned on a CBCT scan. The independent meta-analysis recommends a margin of at least 2 mm even in guided surgery.
Anchorage during placement
The resistance with which the implant seats in the bone can be measured. The decision on immediate loading should be based on this measurement, not on the brand name or the guide.
Supply of parts and the dentist's experience
Being able to get hold of the system in the country where you live keeps a loose screw a small job. A team that uses the same system regularly knows its instruments and its typical problems.
If the loss extends to more than one tooth
If you are missing several teeth, or you have been told there is not enough bone, you can send us the panoramic X-ray or CBCT scan you have through the form. The dentist who will carry out the treatment reads the image, and we will write to you within 24 hours. This is a preliminary assessment; the final decision is made after an examination and a CBCT scan.
What often gets mixed up about DIO
The name of a digital system, several line names and the news of a cancelled sale produce a few misleading shortcuts online.
"DIOnavi is an implant brand"
DIOnavi is not an implant but DIO's digital planning and surgical guide system. The implant that passes through the guide is one of DIO's lines; your card should give not 'DIOnavi' but the implant's line name and size.
"Guided surgery has no deviation"
In a small clinical study in Iran that followed single-tooth implants placed with DIOnavi (9 patients, 14 implants), the mean deviation was found to be 1.74 mm at the tip and 5.07 degrees in angle. In this protocol, in which the implants were placed flapless and loaded on the same day, 2 of the 14 implants were lost in the first three months; the abstract does not separately explain the reason for the losses. The study is small; but it shows that a guide does not eliminate deviation.
"DIO has been sold, it now belongs to a foreign group"
The sale agreement signed in 2022 was cancelled the same year. According to the Korean press, in 2024 the largest shareholder was still DIO Holdings, set up by the fund belonging to Korea's NICE group; H PE, which joined the management in 2024, is a Korean fund too.
"All DIO parts fit one another"
The lines of the same brand can be produced with different connections and sizes; the top part of one line may not fit another. Parts are chosen not by brand name but by line, connection, diameter and length.
"If it did well in a laboratory test, it does well in the mouth too"
In a laboratory study from Seoul National University, the seal between the implant and the healing abutment was measured for six brands; UF(II) was the system that leaked at the lowest pressure. This is a laboratory finding and cannot be translated directly into the outcome in the mouth; the reverse is also true.
What you should have if DIO implants have been fitted
Nobody asks for these documents today; but years from now, in another dentist's chair, they will be the first thing you are asked for.
An implant card with the name of the line
The card should say more than just 'DIO': it should give the line name, such as UF(II), UFIII or FTN, together with the connection type, diameter, length and lot number. If anything is missing, ask the clinic that carried out the treatment to complete it.
The digital plan, if there is one
If DIOnavi was used, a copy of the plan. Compared with an X-ray taken later on, it shows how close to the planned position the implant is seated.
A copy of the barcode
The barcode on the product label carries the number that identifies the implant in ÜTS. Keep it together with your card.
The X-ray from the first day
The X-ray that shows where your bone level was at the start. Only with it can any change be read when it is compared with an X-ray taken years later.
Don't wait if
- If a tooth moves or a screw feels loose. Carrying on chewing with a loose screw can break the screw. Tightening a screw early is a small job; removing a broken one is laborious.
- If there is bleeding, swelling or a bad smell around the implant. Inflammation around an implant often progresses without causing pain. Caught early, it can be stopped; regaining bone that has been lost is much harder. If the swelling is spreading quickly, is accompanied by a fever, or swallowing and breathing become difficult, do not wait: call 112 or go to the nearest A&E department.
- If numbness in the lip, chin or tongue does not pass after the procedure. In the lower jaw, an implant seated close to the nerve can cause numbness. Even if guided surgery was carried out, report this without delay to the dentist who carried out the treatment.
- If you do not know which line was fitted. Call the clinic that carried out the treatment and ask for your record. If there is no record, an attempt will be made to identify the system from an X-ray, but telling apart the lines of the same brand can take time.
How choosing DIO shows up in the quote
The implant's country does not explain the difference in a quote on its own. The total is made up of these items:
- Choice of line and body
- Within the same brand, the lines can differ in cost. Check which line is written in the quote; the phrase 'DIO implant' is not enough on its own.
- Guided surgery
- With a system like DIOnavi, the CBCT scan, the intraoral scan, the digital planning and the production of the guide are separate items of work. Ask whether these are included in the quote.
- Top parts and the prosthesis
- Ready-made parts, patient-specific production or parts for a multi-unit prosthesis, together with the material and workmanship of the bridgework, make up most of the total in full-mouth plans.
- Preparatory procedures and later maintenance
- A graft, a sinus procedure or extractions are separate items. The burden of repairs over the years depends on how easily parts can be obtained.
Frequently asked questions
Which country are DIO implants from?
South Korea. DIO Corporation was founded in 1988, its head office is in Busan and it has been traded on the KOSDAQ exchange since 2000. It began manufacturing dental implants in 2002.
Who owns DIO implants?
Its largest shareholder is DIO Holdings, set up in 2018 by NICE Investment Partners, part of Korea's NICE group. In 2024 a Korean fund called H PE also invested and joined the management. A sale agreement signed in 2022 was cancelled the same year.
What is DIOnavi?
DIO's digital guided surgery system. A CBCT scan and an intraoral scan are combined, the position of the implant is planned on a computer, and the implant is placed with a guide produced according to this plan. It was introduced in 2014; the version for fully edentulous jaws is called DIOnavi Full Arch.
How precise is DIOnavi?
The manufacturer's Turkish website speaks of a deviation of less than 0.9 mm; it does not state at which point of the implant and how this value was measured. In a small independent clinical study examining DIOnavi, the mean deviation was found to be 1.74 mm at the tip of the implant and 5.07 degrees in angle. A meta-analysis examining guided surgery in general also recommends a safety margin of at least 2 mm.
What is the UF II implant?
One of DIO's most widely used lines. According to the document submitted to the FDA, it is made of grade 4 pure titanium and its surface is roughened by sandblasting and acid; it is produced in diameters from 3.8 to 5.5 mm and lengths from 7 to 16 mm. It is stated that it can be loaded immediately when good initial anchorage is achieved.
Where are DIO implants made?
The company's head office is in Busan. According to its history, DIO set up a production company in China in 2017 and acquired the DIO VINA company in Vietnam in 2020. For the product that reaches you, the label on the box and the ÜTS record show the place of manufacture most definitely.
Are DIO implants available in Turkey, and how can I tell they are genuine?
Yes; according to its history, the company set up a company in Turkey in 2020. To check that a product is genuine, ask to see the barcode on the label of the product that will be used: medical devices put on the market in Turkey must be registered in the Product Tracking System. The same information should also appear on your implant card.
Are DIO implants any good?
It is a system from a company that has been producing implants for more than twenty years, many of whose products have been put on the market in the USA through the FDA. But long-term patient follow-up published under the DIO name is limited; most of the publications are laboratory studies or small clinical studies. The outcome, meanwhile, is determined more strongly by planning, load distribution, smoking, diabetes control and maintenance than by the brand.
Do you use DIO?
Our protocol of fixed teeth in 72 hours works with a different class of implant: one-piece corticobasal implants that anchor in the hard outer layer of the jaw. This is not an assessment of conventional systems such as DIO; if there is enough bone and time to wait, they are a sensible choice too. Which one suits you is shown by a CBCT scan.
Sources
- DIO Corporation연혁 (History)
- DIO CorporationDIO NAVI
- DIO Implant TürkiyeDIO Implant
- U.S. Food and Drug Administration510(k) K170608: UF(II) Implant System
- Dealsite나이스투자파트너스, '디오' 밸류업 본격 나섰다 (10 October 2024)
- Dealsite'휴젤 창업자' 홍성범 원장, 임플란트업체 디오 인수 (14 March 2022)
- Edaily[마켓인]임플란트 기업 디오 M&A 무산…"인수자 투자 철회"
- Maxillofacial Plastic and Reconstructive Surgery (PubMed)Digital implant placement accuracy: a clinical study on a fully-guided flapless single-unit immediate-loading protocol.
- Clinical Oral Implants Research (PubMed)The accuracy of static computer-aided implant surgery: A systematic review and meta-analysis.
- International Dental Journal (PubMed)Assessing Microleakage at 2 Different Implant-Healing Abutment Interfaces.
- Türkiye İlaç ve Tıbbi Cihaz Kurumu (TİTCK)Ürün Takip Sistemi (ÜTS)
Related pages
- Making the DecisionDoes the Implant Brand Matter?Where the brand really matters: titanium, surface treatment, connection design, and what decides it: whether spare parts can still be found years later.
- Implant BrandsDental Implant Brands Comparison TableBrands fall into four groups: established global systems, affordable lines in the same groups, Turkish-made and little-known. Origin, strengths, limits, fit.
- Implant BrandsWhere Are Osstem Implants From? South Korea and HiossenOsstem was founded in South Korea in 1997, and Hiossen is its US company. The TS, KS, SS and MS lines, the 2023 ownership change and what your card should say.
- Implant BrandsWhere Are MegaGen Implants Made? AnyOne and AnyRidgeMegaGen was founded in South Korea in 2002; its head office and factory are in Daegu. AnyOne, AnyRidge, ARi, the failed Straumann deal and your implant card.
- Implant BrandsWhere Are Dentium Implants From? SuperLine and ImplantiumDentium was founded in South Korea in 2000 by a dentist. The SuperLine, Implantium and bright lines, how their connections differ and what your card should say.
- Close-upDoes Guided Implant Planning Really Change the Result?Intraoral scans, CBCT scans and a surgical guide measurably cut positioning deviation. What this millimetre-level gain means long term is far less clear.
- The ProcessFlapless (Stitch-Free) Implants: Who Suits Them, What Risks?With flapless implants the gum is not opened and the bone is not seen. Less pain, shorter surgery, similar survival; deviation risk and why a guide matters.
- Implant BrandsWhich Country Are BioHorizons Implants From? Laser-LokBioHorizons is a US brand founded in Birmingham, Alabama in 1994, now part of Henry Schein. What Laser-Lok is, the independent evidence and your implant card.
- Implant BrandsWhich Country Is Medentika From? Its Link to StraumannMedentika is a German company in the Straumann Group. Its own implants, top parts compatible with other brands, and the original versus compatible evidence.
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