FDA applicant

Anspach Mfg., Inc.

Lake Park, FL3 decisions1991–19940 recalls

FDA records 3 decisions for Anspach Mfg., Inc. (Lake Park, FL) from 1991 to 1994: 3 510(k) clearances. Most are in product codes HSZ (Instrument, Surgical, Orthopedic, Pneumatic…) and HWC (Screw, Fixation, Bone). 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 Anspach Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anspach Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anspach Mfg., 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 “Anspach”

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

The Anspach Effort, Inc. 60 Anspach Fixation Systems 1

Anspach Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Anspach”