FDA applicant

Fray Products Corp.

Tonawanda, NY1 decision1992–19923 recalls

FDA records 1 decision for Fray Products Corp. (Tonawanda, NY) in 1992: 1 510(k) clearance. All are in product code MDM (Instrument, Manual, Surgical, General Use). 3 recalls are 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 Fray Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fray Products Corp. since 2007.

Recalls per year

3in 2013

2007high 3 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Fray Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?