FDA Device Intelligence
Home › Peter Brasseler Holdings, LLC › Brasseler USA

Brasseler USA

Peter Brasseler Holdings, LLC · Model 5024417U0 · UDI-DI 00887919718192

DZP Prescription
10
510(k) clearances
37
Adverse events
0
Recalls
121
Facilities

Description

WSMR1.0 (F) MARGIN REFINE 5P

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.