FDA applicant

Avid Medical, Inc.

Toano, VA2 decisions2000–20001 recall

FDA records 2 decisions for Avid Medical, Inc. (Toano, VA) in 2000: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and HEE (Set, Anesthesia, Paracervical). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Avid Medical, Inc. since 2007.

Recalls per year

1in 2018

2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Avid”

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

Avid N.I.T., Inc. 9 Avid Care Corp. 2

Avid Medical, 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 “Avid”