Not currently registered with FDA under this name
Atrix Laboratories, Inc.
Fort Collins, CO, United States. Named as applicant on 3 dental 510(k) clearances between 1996 and 2000. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 31996–2000
- Markets registered in
- 32 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1990–2026
Registered in 3 markets
Where regulators' registries name Atrix Laboratories, Inc. 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 | Atrix Laboratories, Inc. | 3 clearances | 1996–2000 | Below |
| South Korea | MFDS | Manufacturer | Atrix Laboratories,Inc. | 1 | 2000–2000 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | ATRIX LABORATORIES, INC. | 1 | 1999–1999 | 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 Atrix Laboratories, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 13 Sep 2000 | K994137 | ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINE | LYC Synthetic Bone Grafting Material |
| 8 Sep 1998 | K982865 | ATRISORB BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER KIT | NPK Intraoral Synthetic Barrier |
| 21 Mar 1996 | K955838 | ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR) | NPK Intraoral Synthetic Barrier |
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.