FDA applicant

Avid N.I.T., Inc.

Oldsmar, FL9 decisions1995–20020 recalls

FDA records 9 decisions for Avid N.I.T., Inc. (Oldsmar, FL) from 1995 to 2002: 9 510(k) clearances. Most are in product codes IWJ (System, Applicator, Radionuclide, Manual) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). No 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, anesthesiology panel, where it files most

How often FDA has decided Avid N.I.T., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Avid N.I.T., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Avid N.I.T., 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 Care Corp. 2 Avid Medical, Inc. 2

Avid N.I.T., 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?

Other applicant names beginning “Avid”