FDA Device Intelligence
Home › Joimax GmbH › endo-elevator

endo-elevator

Joimax GmbH · Model DEE264519C · UDI-DI 04250337114475

GEG Prescription
10
510(k) clearances
39
Adverse events
0
Recalls
228
Facilities

Description

Endo-Elevator blunt

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.