FDA applicant

Anchor Medical Technologies

Irvine, CA1 decision2001–20010 recalls

FDA records 1 decision for Anchor Medical Technologies (Irvine, CA) in 2001: 1 510(k) clearance. All are in product code 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, orthopedic panel, where it files most

How often FDA has decided Anchor Medical Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anchor Medical Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anchor Medical 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 “Anchor”

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

Anchor Products Co. 7 Anchor Innovation Medical (A.I.M.) 2 Anchor Implants, Ltd. 2 Anchor Implant Systems, Inc. 1 Anchor Innovation Medical, Inc. 1 Anchor Brush Co., Inc. 1

Anchor Medical Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Anchor”