FDA applicant

Procare C/O Wiley, Rein & Fielding

Washington, DC1 decision1987–19870 recalls

FDA records 1 decision for Procare C/O Wiley, Rein & Fielding (Washington, DC) in 1987: 1 510(k) clearance. All are in product code LHD (Device, Fertility Diagnostic, Proceptive). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Procare C/O Wiley, Rein & Fielding’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Procare C/O Wiley, Rein & Fielding since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Procare C/O Wiley, Rein & Fielding by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Procare C/O Wiley, Rein & Fielding’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 “Procare”

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

Procare Industrial Co., Limited 1

Procare C/O Wiley, Rein & Fielding

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Procare”