FDA Device Intelligence
Home › ACE SURGICAL SUPPLY CO., INC. › ACE

ACE

ACE SURGICAL SUPPLY CO., INC. · Model 0031400 · UDI-DI 00614950009152

FPX Prescription
10
510(k) clearances
64
Adverse events
1
Recalls
31
Facilities

Description

ADMIN SET IV 68" CONVERT PIN W/FLASH BULB 15DPS/MIN 50/CA

Recalls

DateFirmReason
2013-07-18Aspen Surgical Products, Inc.Aspen Surgical is recalling Wound Closures because firm could not confirm sterility, after FDA sampling indicated the product may not be sterile. Using the recalled product could l

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.