Not currently registered with FDA under this name
Collagen Corp.
Palo Alto, CA, United States. Named as applicant on 8 dental 510(k) clearances between 1988 and 1990. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 81988–1990
- Markets registered in
- 32 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1980–2026
Registered in 3 markets
Where regulators' registries name Collagen Corp. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Collagen Corp. | 8 clearances | 1988–1990 | Below |
| South Korea | MFDS | Manufacturer | Collagen Corporation | 1 | 1999–1999 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | COLLAGEN CORPORATION | 1 | 1991–1991 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Collagen Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 21 Dec 1990 | K904671 | QAR HANDPIECE | EFB Dental Air-Powered Handpiece |
| 9 Nov 1990 | K904228 | OSSEODENT DENTAL ATTACHMENTS (NON-ANGLED) | DZE Root-Form Endosseous Implant |
| 21 Jun 1990 | K901600 | OSSEOTITE IRRIGATION UNIT | EFS Oral Irrigation Unit |
| 19 Apr 1990 | K900275 | OSSEODENT DENTAL ATTACHMENT, IGLOO MAGNET | DZE Root-Form Endosseous Implant |
| 4 Apr 1990 | K895462 | OSSEODENT DENTAL ATTACHMENTS | DZE Root-Form Endosseous Implant |
| 28 Mar 1990 | K895463 | OSSEODENT(R) PRECISION DENTAL ATTACHMENTS | DZE Root-Form Endosseous Implant |
| 4 Oct 1989 | K894331 | OSSEODENT SURGICAL KIT | DZE Root-Form Endosseous Implant |
| 26 Aug 1988 | K883322 | DENTAL HAND INSTRUMENTS | EKJ Operative Burnisher |
Some of these clearances are listed with FDA today by another company: ZimVie US Corp LLC (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.