FDA applicant

Cooper Surgical

Huntington, CT6 decisions2002–20260 recalls

FDA records 6 decisions for Cooper Surgical (Huntington, CT) from 2002 to 2026: 6 510(k) clearances. Most are in product codes MQF (Catheter, Assisted Reproduction) and KGI (Densitometer, Bone). Its devices cite 7 predicates, 0 of them its own earlier devices. 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Cooper Surgical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cooper Surgical’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 “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 Medical Corp. 5 Cooper Laboratories 1 Cooper Surgical/Aesthete 1 Cooper Diagnostics, Inc. 1 The Cooper Companies 1

Cooper Surgical

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cooper”