Taiject Medical Device Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Taiject Medical Device Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Taiject Medical Device Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Historical record: 4 cleared submissions from 2002 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Taiject Medical Device Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Taiject Medical Device Co., Ltd.
4 devices
Cleared
Sep 22, 2004
TMD 0.5ML SAFETY SYRINGE (FA18 SERIES 0.5ML/FA58 SERIES U-100 INSULIN/FA78...
General Hospital
14d
Cleared
May 02, 2003
TMD 1ML SAFETY SYRINGE (FA11 SERIES 1ML/FA51 SERIES U-100 INSULIN/FA71 SERIES...
General Hospital
29d
Cleared
Nov 07, 2002
TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML)
General Hospital
23d
Cleared
Sep 12, 2002
TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)
General Hospital
59d