FDA applicant

Cryomedics, Inc.

Bridgeport, CT7 decisions1980–19850 recalls

FDA records 7 decisions for Cryomedics, Inc. (Bridgeport, CT) from 1980 to 1985: 7 510(k) clearances. Most are in product codes GEH (Unit, Cryosurgical, Accessories) and DWS (Instruments, Surgical, Cardiovascular). 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 Cryomedics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cryomedics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cryomedics, 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

Cryomedics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?