Medical Device Manufacturer · US , Las Vegas , NV

Clinical House Europe GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

Recent clearances: PerioType Rapid, PERIOTYPE X-PERT

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Clinical House Europe GmbH Dental ✕

2 devices

1-2 of 2

Cleared Aug 07, 2015

PerioType Rapid

Cleared Apr 26, 2013

PERIOTYPE X-PERT