FDA applicant

Hall Surgical, Division of Zimmer, Inc.

`Anta Barbara, CA8 decisions1985–19941 recall

FDA records 8 decisions for Hall Surgical, Division of Zimmer, Inc. (`Anta Barbara, CA) from 1985 to 1994: 8 510(k) clearances. Most are in product codes HRX (Arthroscope) and HWE (Instrument, Surgical, Orthopedic, Ac-Powered…). 1 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 Hall Surgical, Division of Zimmer, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hall Surgical, Division of Zimmer, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hall Surgical, Division of Zimmer, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hall Surgical, Division of Zimmer, Inc.’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 “Hall”

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

Hall Laboratories, Inc. 2 Hall-Woodroof, Inc. 2 Hall-Tech 2 Hall Medical Laboratories 2 Hall/Mccollum Laboratories, Inc. 2

Hall Surgical, Division of Zimmer, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Hall”