FDA Device Intelligence
HomeAesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model DE427R · UDI-DI 04038653228386

EIY Prescription
5
510(k) clearances
18
Adverse events
0
Recalls
187
Facilities

Description

HOLLENBACK Finishing Instrument, angled, 7" (175 mm), double ended, hexagonal handle, Fig. 1/2

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.