FDA applicant

Amsco Sterile Recoveries, Inc.

Clearwater, FL12 decisions1992–19940 recalls

FDA records 12 decisions for Amsco Sterile Recoveries, Inc. (Clearwater, FL) from 1992 to 1994: 12 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and FYC (Gown, Isolation, Surgical). 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 Amsco Sterile Recoveries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Amsco Sterile Recoveries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Amsco Sterile Recoveries, 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 “Amsco”

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

Amsco Co. 19 Amsco Hospital Products Co. 1 Amsco American Sterilizer Co. 1 Amsco Intl., Inc. 1

Amsco Sterile Recoveries, 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?

Other applicant names beginning “Amsco”