FDA Device Intelligence
HomeSURGICAL TECHNOLOGY LABORATORIES INC › Pureform

Pureform

SURGICAL TECHNOLOGY LABORATORIES INC · Model 3NDR01 · UDI-DI 00850987007130

FZE Prescription
1
510(k) clearances
211
Adverse events
0
Recalls
26
Facilities

Description

"3NDR01 3mm Rounded Nasal Dorsum - Small"

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.