FDA applicant

Angiotech Medical Device Technologies

Gainesville2 decisions2000–20010 recalls

FDA records 2 decisions for Angiotech Medical Device Technologies (Gainesville) from 2000 to 2001: 2 original PMA approvals. Most are in product codes PMX (Absorbable Collagen Hemostatic Agent With…) and NBE (Sealant, Polymerizing). 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 Angiotech Medical Device Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Angiotech Medical Device Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Angiotech”

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

Angiotech 7 Angiotech Pharmaceuticals, Inc. 1

Angiotech Medical Device Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Angiotech”