Medical Device Manufacturer · TW , Kaohsiung

Peng Lim Enterprise Co., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Recent clearances: HIGH SPEED AIR TURBINE HANDPIECE, MODELS SUPER-AIR AND SUPER-QD SERIES, LED PROLUX 770

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Peng Lim Enterprise Co., Ltd. Dental ✕

2 devices

1-2 of 2

Cleared Dec 14, 2006

HIGH SPEED AIR TURBINE HANDPIECE, MODELS SUPER-AIR AND SUPER-QD SERIES

Cleared Sep 14, 2006

Data Source

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

Last updated: Sep 28, 2026