FDA applicant

Amsco Co.

Mchenry, IL19 decisions1977–19920 recalls

FDA records 19 decisions for Amsco Co. (Mchenry, IL) from 1977 to 1992: 19 510(k) clearances. Most are in product codes GET (Motor, Surgical Instrument, Pneumatic Powered) and JOJ (Indicator, Physical/Chemical Sterilization…). 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 Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Amsco Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Amsco Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Amsco”

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

Amsco Sterile Recoveries, Inc. 12 Amsco Hospital Products Co. 1 Amsco American Sterilizer Co. 1 Amsco Intl., Inc. 1

Amsco Co.

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”