Carwild Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carwild Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Carwild Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1979 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Carwild Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carwild Corp.
6 devices
Cleared
Aug 06, 1992
LAP SPONGES, MODIFIED
General & Plastic Surgery
378d
Cleared
Jul 23, 1992
DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED
General & Plastic Surgery
364d
Cleared
May 31, 1984
SUTURE REMOVAL KITS STERILE
General & Plastic Surgery
213d
Cleared
Nov 13, 1979
LAP SPONGES
General & Plastic Surgery
53d
Cleared
Nov 05, 1979
DISPOSABLE SPECIALITY SPONGES
General & Plastic Surgery
45d
Cleared
Nov 05, 1979
NEUROLOGICAL SPONGES (PATTIES)
General & Plastic Surgery
45d