Medical Device Manufacturer · US , Stoughton , MA

Std Mfg., Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1993

Recent clearances: CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEM, CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEM, MODIFICATION TO VASCULAR CLOSURE DEVICE

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

Std Mfg., Inc. has 6 FDA 510(k) cleared medical devices. Based in Stoughton, US.

Historical record: 6 cleared submissions from 1993 to 2003. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Std Mfg., Inc. Filter by specialty or product code using the sidebar.

Std Mfg., Inc. is one of 25841 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Std Mfg., Inc.

6 devices

1-6 of 6

Cleared Apr 10, 2003

CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEM

Orthopedic · 204d

Cleared Aug 01, 2002

CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEM

Orthopedic · 80d

Cleared Aug 23, 2001

MODIFICATION TO VASCULAR CLOSURE DEVICE

General & Plastic Surgery · 29d

Cleared Dec 08, 2000

VASCULAR CLOSURE DEVICE

General & Plastic Surgery · 59d

Cleared Mar 07, 2000

SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEM

General & Plastic Surgery · 13d

Cleared Jun 01, 1993

STD IRRIGATION PUMP

General & Plastic Surgery · 126d