CAMLOG
Also known as: Camlog, CAMLOG Biotechnologies GmbH, CONELOG
A Swiss-headquartered implant brand within Henry Schein’s oral reconstruction division, offering the CAMLOG, CONELOG, CERALOG and iSy systems.
Key facts
| Manufacturer | Henry Schein, Inc.Verified spec[1][2][3] |
|---|---|
| Parent company | Henry Schein, Inc., Melville, New YorkVerified spec[2] |
| Country | Switzerland, with manufacturing in GermanyVerified spec[4][1] |
| Headquarters | CAMLOG Biotechnologies GmbH, Grosspeteranlage 29, 4052 Basel, SwitzerlandVerified spec[4][1] |
| Founded | Manufacturer documentation not located(No founding year is stated on the company pages we were able to reach) |
| Ownership | Operates under a Henry Schein division that Camlog names the Global Dental Surgical Group and Henry Schein names the Global Oral Reconstruction Group; it has worked with BioHorizons since 2016 as BioHorizons CamlogVerified spec[1][5][2]The two divisional names appear to describe the same organisation; we have recorded both rather than choose between them |
| Prosthetic ecosystem | Product lines are CAMLOG with the Tube-in-Tube connection, CONELOG with a conical connection and platform switching, the CERALOG zirconia line and the reduced-component iSy systemManufacturer-reported[1] |
| Geographic availability | Distributed in more than 90 countries; implants are manufactured at ALTATEC GmbH in Wimsheim, GermanyManufacturer-reported[1] |
| manufacturingCountry | SwitzerlandVerified spec[6]Country of the FDA-registered device establishment, which may differ from the brand’s home country. |
Overview
Regulatory record
Read this before drawing conclusions. A clearance or certificate means a device may legally be sold in a market. It is not a finding that the implant performs well, and it is not a comparison against other implants. In particular, FDA "clearance" is not FDA "approval" — clearance means the FDA accepted the device as substantially equivalent to one already on the market. What these actually mean →
Other1 record
Registered device establishment in Switzerland. Registration records where a device is made or handled; it is not a clearance, an approval, or any assessment of the product.
| Number | Device | Holder | Date |
|---|---|---|---|
| 3007283751 | — | CAMLOG Biotechnologies GmbH | — |
Clearance records for CAMLOG were retrieved from the issuing authority's own database, not from the manufacturer's marketing material. We attribute a clearance to a brand only when the filing holder belongs to that brand's corporate family — third-party clearances for compatible components are excluded, because they belong to the company that made the component, not to CAMLOG.
Sources
Numbers match the citations beside each claim above.
Primary sources
- [1]Company — CAMLOG — CAMLOG Biotechnologies GmbH. Accessed 2026-07-21.
- [2]Henry Schein, Inc. — Annual Report on Form 10-K for the year ended 27 December 2025 — U.S. Securities and Exchange Commission (EDGAR), 2026. Accessed 2026-07-21.
- [3]Brands of BioHorizons Camlog Group — BioHorizons Camlog Group. Accessed 2026-07-21.
- [4]Camlog worldwide — international distribution — CAMLOG Biotechnologies GmbH. Accessed 2026-07-21.
- [5]About us — BioHorizons Camlog Group — BioHorizons Camlog Group. Accessed 2026-07-21.
- [6]openFDA — Device registrations and listings — US Food and Drug Administration. Accessed 2026-07-22.