Z-Medica, LLC
Z-Medica, LLC holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2022, with 3 FDA device recalls on record.
Top product codes for Z-Medica, LLC
FDA recalls by Z-Medica, LLC
- Z-0211-2022 — QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200
- Z-0925-2018 — QuikClot TraumaPad, Part# 460 a topical dressing for local management of bleeding wounds such as cuts, lacerations, and abrasions. It may also be used for temporary treatment of severely bleeding wounds such as surgical wounds (operative, postoperative, dermatological, etc.) and traumatic injuries
- Z-2612-2017 — QuikClot TraumaPad, , sterile, soft, white, X-ray detectable hemostatic dressing Part Number 460 Manufactured by Z-Medica, LLC 4 Fairfield Boulevard, Wallingford, CT 06492 USA For use as a topical dressing for local management of bleeding wounds such as cuts, lacerations, and abrasions. It may also be used for temporary treatment of severely bleeding wounds such as surgical wounds (operative, postoperative, dermatological, etc.) and traumatic injuries
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Z-Medica, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.