FDA Device Intelligence
Home › Zoll-Dental › ZOLL-DENTAL

ZOLL-DENTAL

Zoll-Dental · Model Z-6801 · UDI-DI 00840105220145

EAX
10
510(k) clearances
47
Adverse events
1
Recalls
371
Facilities

Description

Micro-Surgical Mirror Round

Recalls

DateFirmReason
2021-03-23Sunstar Americas, Inc.Product may be contaminated with Burkholderia contaminans.

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.