Medical Device Manufacturer · US , Morgan Hill , CA

Aesthera Corporation - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005

Recent clearances: ISOLAZ, AESTHERA PHOTOPNEUMATIC (PPX) SYSTEM, AIP INTENSE PULSED LIGHT SYSTEM

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesthera Corporation General & Plastic Surgery ✕

3 devices

1-3 of 3

Cleared Jan 09, 2009

General & Plastic Surgery · 24d

Cleared Sep 07, 2006

AESTHERA PHOTOPNEUMATIC (PPX) SYSTEM

General & Plastic Surgery · 49d

Cleared Apr 27, 2005

AIP INTENSE PULSED LIGHT SYSTEM

General & Plastic Surgery · 321d