FDA applicant

Baxter Interwoven Offsite

Tampa, FL1 decision1992–19920 recalls

FDA records 1 decision for Baxter Interwoven Offsite (Tampa, FL) in 1992: 1 510(k) clearance. All are in product code FYA (Gown, Surgical). 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, general and plastic surgery panel, where it files most

How often FDA has decided Baxter Interwoven Offsite’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Baxter Interwoven Offsite since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Baxter”

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

Baxter Healthcare Corp 574 Baxter Diagnostics, Inc. 72 Baxter Edwards 11 Baxter Bentley Laboratories, Inc. 3 Baxter Healthcare Corportation 3 Baxter Healthcare Corporation - Renal Division 2 Baxter/ Synovis Micro Companies Alliance, Inc. 2 Baxter Healthcare Corp/ Excel Medical 1 Baxter Centre For Medical Research 1 Baxter Healthcare Corproration 1 Baxter Corp. 1 Baxter Healthcare Corp., Bioscience 1

Baxter Interwoven Offsite

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Baxter”