FDA Device Intelligence
Home › AMBLER SURGICAL CORP. › Ambler Surgical

Ambler Surgical

AMBLER SURGICAL CORP. · Model Tenolysis pulley dilator · UDI-DI 00190660203443

HNW Prescription
3
510(k) clearances
50
Adverse events
0
Recalls
139
Facilities

Description

Tenolysis pulley dilator, double-ended, 3.0mm-5.0mm and 4.0mm-6.0mm, round handle

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.