Medical Device Manufacturer · DE , Teltow

Celon AG Medical Instruments - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Recent clearances: OLYMPUS ESG-100, MODEL WB991046, CELON ENT SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Celon AG Medical Instruments General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared May 08, 2008

OLYMPUS ESG-100, MODEL WB991046

General & Plastic Surgery · 177d

Cleared Sep 26, 2003

CELON ENT SYSTEM

General & Plastic Surgery · 15d

Data Source

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

Last updated: Sep 30, 2026