510(k) Report

FDA applicant

Renaissance Pharmaceutical, Inc.

Glenbrook, NV4 decisions1994–19960 recalls

FDA records 4 decisions for Renaissance Pharmaceutical, Inc. (Glenbrook, NV) from 1994 to 1996: 4 510(k) clearances. All are in product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…). 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 Renaissance Pharmaceutical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Renaissance Pharmaceutical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Renaissance”

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