FDA Device Intelligence
HomeRZ-Medizintechnik GmbH › RZ Medizintechnik GmbH

RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 430-105-001 · UDI-DI 04049197319263

KAD Prescription
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities

Description

Blair Cleft Palate Elevator L-shaped, rounded, blunt, 7x15mm 190mm, 7 1/2"

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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.