FDA applicant

Synovis Life Technologies. Inc. (A Subsidiary of Baxter

St. Paul, MN1 decision2021–20210 recalls

FDA records 1 decision for Synovis Life Technologies. Inc. (A Subsidiary of Baxter (St. Paul, MN) in 2021: 1 510(k) clearance. All are in product code FTM (Mesh, Surgical). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Synovis Life Technologies. Inc. (A Subsidiary of Baxter’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Synovis Life Technologies. Inc. (A Subsidiary of Baxter by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Synovis Life Technologies. Inc. (A…’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 “Synovis”

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

Synovis Life Technologies, Inc. 9 Synovis Surgical Innovations 9 Synovis Micro Companies Alliance, Inc. 5 Synovis Orthopedic & Woundcare 3 Synovis Orthopedic and Woundcare, Inc. 1 Synovis Micro Companies Alliance A Subsidiary of… 1 Synovis Life Technologies, Inc. (Baxter International… 1

Synovis Life Technologies. Inc. (A Subsidiary of Baxter

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Synovis”