Paonan Biotech Co., Ltd.

FDA Regulatory Profile

Paonan Biotech Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 24, 2023.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220261NEST-C Interbody SystemApril 24, 2023
K182285PK High Tibial Osteotomy Correction SystemJune 20, 2019
K180230NEST Interbody SystemJanuary 25, 2019
K180228II-Type Intervertebral SpacerJanuary 11, 2019
K180226TREND II Spinal Fixation System- STEP SeriesJuly 25, 2018
K161225Paonan Armstrong Posterior Spinal Fixation SystemAugust 11, 2017