FDA applicant

Perimeter Medical, Inc.

Tucson, AZ5 decisions1985–19850 recalls

FDA records 5 decisions for Perimeter Medical, Inc. (Tucson, AZ) in 1985: 5 510(k) clearances. Most are in product codes GCY (Apparatus, Suction, Single Patient Use…) and GBX (Catheter, Irrigation). 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 Perimeter Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perimeter Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Perimeter Medical, 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 “Perimeter”

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

Perimeter Medical Imaging, Inc. 3 Perimeter Medical Imaging Ai, Inc. 2

Perimeter Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Perimeter”