Medical Device Manufacturer · US , Baltimore , MD

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

2 submissions · 2 cleared · Since 1998

Recent clearances: AUTOGENESIS AUTOMATOR, MODEL M1000, AUTOGENESIS AUTOMATOR 2000 MODEL NUMBER SC2000

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Autogenesis, Inc. Orthopedic ✕

2 devices

1-2 of 2

Cleared Dec 05, 2001

AUTOGENESIS AUTOMATOR, MODEL M1000

Orthopedic · 19d

Cleared May 20, 1998

AUTOGENESIS AUTOMATOR 2000 MODEL NUMBER SC2000

Orthopedic · 30d