Paonan Biotech Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Paonan Biotech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NEST-C Interbody System, PK High Tibial Osteotomy Correction System, NEST Interbody System
6
Total
6
Cleared
0
Denied
Paonan Biotech Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Last cleared in 2023. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Paonan Biotech Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paonan Biotech Co., Ltd.
6 devices
Cleared
Apr 24, 2023
NEST-C Interbody System
Orthopedic
448d
Cleared
Jun 20, 2019
PK High Tibial Osteotomy Correction System
Orthopedic
301d
Cleared
Jan 25, 2019
NEST Interbody System
Orthopedic
364d
Cleared
Jan 11, 2019
II-Type Intervertebral Spacer
Orthopedic
350d
Cleared
Jul 25, 2018
TREND II Spinal Fixation System- STEP Series
Orthopedic
180d
Cleared
Aug 11, 2017
Paonan Armstrong Posterior Spinal Fixation System
Orthopedic
452d