Baui Biotech Co., Ltd.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Baui Biotech Co., Ltd.” (first 2017, latest 2024), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 266 days. Since 2017 the median was 266 days, against 89 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2017 | 1 | 266 |
| 2018 | 0 | — |
| 2019 | 2 | 174 |
| 2020 | 1 | 329 |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 1 | 24 |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Baui Biotech Co., Ltd. took a median 266 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 89 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| NKB | Thoracolumbosacral Pedicle Screw System | 4 | 4 |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 1 | 1 |
Review panels
- Orthopedic (5)
Most recent Baui Biotech Co., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K242899 | NOVA Minimally Invasive System | NKB | 2024-10-17 | 24 |
| K191353 | COMET Lumbar Interbody Fusion Cage | MAX | 2020-04-14 | 329 |
| K191494 | Facilis Spinal System | NKB | 2019-08-12 | 68 |
| K182416 | NOVA Minimally Invasive System | NKB | 2019-06-11 | 280 |
| K161231 | Facilis Spinal System | NKB | 2017-01-23 | 266 |
Recalls
openFDA lists no recalls under a recalling firm named Baui Biotech Co., Ltd..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Baui Biotech Co., Ltd.?
FDA lists 5 510(k) clearances under the applicant name “Baui Biotech Co., Ltd.” (first 2017, latest 2024), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Baui Biotech Co., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Baui Biotech Co., Ltd. is 266 days. Since 2017: 266 days, versus 89 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Baui Biotech Co., Ltd.?
The most frequent FDA product codes under this applicant name are NKB (Thoracolumbosacral Pedicle Screw System, 4); MAX (Intervertebral Fusion Device With Bone Graft, Lumbar, 1).
Next steps
- See all 5 Baui Biotech Co., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code NKB, Baui Biotech Co., Ltd.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.