FDA Device Intelligence
Home › Schobell Industrial Ltda › Quinelato

Quinelato

Schobell Industrial Ltda · Model QO.826.24 · UDI-DI 07898506853687

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
246
Facilities

Description

Pliers Steinmann 24 "

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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.