Medical Device Manufacturer · US , Stoughton , MA

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

6 submissions · 6 cleared · Since 1993

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.

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