FDA applicant

Precision Therapeutics, Inc.

Las Vegas, NV2 decisions1987–19870 recalls

FDA records 2 decisions for Precision Therapeutics, Inc. (Las Vegas, NV) in 1987: 2 510(k) clearances. Most are in product codes HMP (Pad, Eye) and HOY (Shield, Eye, Ophthalmic (Including Sunlamp…). 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 Precision Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precision Therapeutics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Precision Therapeutics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?