FDA Device Intelligence
Home › SONTEC INSTRUMENTS, INC. › DRILL TUBE

DRILL TUBE

SONTEC INSTRUMENTS, INC. · Model 1103-16835 · UDI-DI 00192896093829

LXI Prescription
8
510(k) clearances
74
Adverse events
0
Recalls
44
Facilities

Description

DRILL TUBE

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.