FDA applicant

Cooper Surgical/Aesthete

Paso Robles, CA1 decision1989–19890 recalls

FDA records 1 decision for Cooper Surgical/Aesthete (Paso Robles, CA) in 1989: 1 510(k) clearance. All are in product code NAD (Dressing, Wound, Occlusive). 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 Cooper Surgical/Aesthete’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cooper Surgical/Aesthete since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cooper Surgical/Aesthete’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 “Cooper”

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

Cooper Lasersonics, Inc. 54 Cooper Biomedical, Inc. 19 Cooper-Hewitt Electric Co. 8 Cooper Medical Devices Corp. 7 Cooper Surgical 6 Cooper Medical Corp. 5 Cooper Laboratories 1 Cooper Diagnostics, Inc. 1 The Cooper Companies 1

Cooper Surgical/Aesthete

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cooper”