FDA Device Intelligence
Home › SONTEC INSTRUMENTS, INC. › EPKER-TYPE OSTEOTOME

EPKER-TYPE OSTEOTOME

SONTEC INSTRUMENTS, INC. · Model 330-336 · UDI-DI 00192896029675

HWM Prescription
3
510(k) clearances
767
Adverse events
0
Recalls
254
Facilities

Description

EPKER-TYPE OSTEOTOME FULL CURVE JAW

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.