FDA Device Intelligence
HomeRestor3d, Inc. › Ossera™ AFX Instrumentation

Ossera™ AFX Instrumentation

Restor3d, Inc. · Model 6744-4050-N · UDI-DI 00840097526331

SAI Prescription
1
510(k) clearances
2
Adverse events
0
Recalls
5
Facilities

Description

Ossera™ AFX Trial, Rectangle, 41x31x50

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.