FDA Device Intelligence
Home › PRODONT-HOLLIGER › PRODONT-HOLLIGER

PRODONT-HOLLIGER

PRODONT-HOLLIGER · Model MP4305PH · UDI-DI 03665224016472

EAX
10
510(k) clearances
47
Adverse events
1
Recalls
374
Facilities

Description

micromirror css pure reflect ø5mm

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.