FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model DB866R · UDI-DI 04046963890629

EIX Prescription
9
510(k) clearances
10
Adverse events
0
Recalls
170
Facilities

Description

Periodontometer, angled, 6 3/4" (170 mm), double ended, Golfball design handle, UPM (PCP 11,5 C + UNC 15)

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.