FDA Device Intelligence
Home › Osstell AB › Osstell SmartPeg Type 113

Osstell SmartPeg Type 113

Osstell AB · Model Osstell SmartPeg Type 113 · UDI-DI 09010522002575

EKX Prescription
1
510(k) clearances
736
Adverse events
0
Recalls
92
Facilities

Description

ISQ Measurement Peg

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.