Medical Device Manufacturer · US , Washington , DC

Mani, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2005

Recent clearances: MANI NEEDLE & SUTURE PACK (NYLON), MANI NEEDLE & SUTURE PACK (SILK), MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mani, Inc. General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared May 19, 2006

MANI NEEDLE & SUTURE PACK (NYLON)

General & Plastic Surgery · 141d

Cleared May 19, 2006

MANI NEEDLE & SUTURE PACK (SILK)

General & Plastic Surgery · 141d

Cleared Mar 14, 2006

MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)

General & Plastic Surgery · 75d

Cleared Dec 05, 2005

MANI NEEDLE & SUTURE PACK

General & Plastic Surgery · 315d