FDA applicant

Atrix Laboratories, Inc.

Fort Collins, CO3 decisions1996–20001 recall

FDA records 3 decisions for Atrix Laboratories, Inc. (Fort Collins, CO) from 1996 to 2000: 3 510(k) clearances. Most are in product codes NPK (Barrier, Synthetic, Intraoral) and LYC (Bone Grafting Material, Synthetic). Its devices cite 2 predicates, 2 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Atrix Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Atrix Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Atrix Laboratories, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Atrix Laboratories, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Atrix”

FDA records each applicant name separately; these may or may not be the same firm.

Atrix 2

Atrix Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Atrix”