Medical Device Manufacturer · US , Houston , TX

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

2 submissions · 2 cleared · Since 2014

Recent clearances: SMARTGRAFT 200 SYSTEM, SMARTGRAFT 30 SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Oct 28, 2014

SMARTGRAFT 200 SYSTEM

General & Plastic Surgery · 125d

Cleared Sep 24, 2014

SMARTGRAFT 30 SYSTEM

General & Plastic Surgery · 103d