FDA Device Intelligence
HomeAesculap AG › ERGOPLANT

ERGOPLANT

Aesculap AG · Model DX360T · UDI-DI 04046963322199

EMK Prescription
1
510(k) clearances
1
Adverse events
0
Recalls
129
Facilities

Description

ERGOPLANT Universal Curette, 6 3/4", (170 mm), non-sterile, reusable

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.