FDA Device Intelligence
Home › Adler, Inc. › Adler Instrument Company

Adler Instrument Company

Adler, Inc. · Model 35-0397 · UDI-DI 00810123200740

HWM Prescription
3
510(k) clearances
749
Adverse events
0
Recalls
254
Facilities

Description

LAMBOTTE MINI OSTEO 5 STR 14MM

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.