Medical Device Manufacturer · US , Bozeman , MT

Quantel Derma GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Recent clearances: EXELO2, MODEL 4010, LEDA

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Quantel Derma GmbH General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Oct 29, 2009

EXELO2, MODEL 4010

General & Plastic Surgery · 233d

Cleared Aug 28, 2009

General & Plastic Surgery · 158d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Oct 02, 2026