Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in TaiwanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Paonan Biotech with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2023: NEST-C Interbody System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 24, 2023 | NEST-C Interbody SystemK220261 · ODP | 510(k) clearances |
| Jun 20, 2019 | PK High Tibial Osteotomy Correction SystemK182285 · KTW | 510(k) clearances |
| Jan 25, 2019 | NEST Interbody SystemK180230 · MAX | 510(k) clearances |
| Jan 11, 2019 | II-Type Intervertebral SpacerK180228 · MAX | 510(k) clearances |
| Jul 25, 2018 | TREND II Spinal Fixation System- STEP SeriesK180226 · NKB | 510(k) clearances |
| Aug 11, 2017 | Paonan Armstrong Posterior Spinal Fixation SystemK161225 · NKB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
