Nanjing Bestview Laser S&T Co., Ltd.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Nanjing Bestview Laser S&T Co., Ltd.” (first 2024, latest 2026), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 90 days. Since 2017 the median was 90 days, against 90 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 |
|---|---|---|
| 2024 | 1 | 90 |
| 2025 | 2 | 103 |
| 2026 | 2 | 67 |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Nanjing Bestview Laser S&T Co., Ltd. took a median 90 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 90 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | 4 | 4 |
| ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | 1 | 1 |
Review panels
Most recent Nanjing Bestview Laser S&T Co., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K260974 | CO2 Laser Machine (Monica-I,Monica-II) | GEX | 2026-05-07 | 44 |
| K260153 | Q-Switched Nd: YAG Laser System (Glamor Q) | GEX | 2026-04-20 | 90 |
| K251919 | Thulium Laser System (Deluxlase) | GEX | 2025-09-26 | 95 |
| K250465 | CO2 Laser Machine (Lume) | GEX | 2025-06-09 | 111 |
| K242440 | Intense Pulsed Light Treatment System (LK-PT) | ONF | 2024-11-14 | 90 |
Recalls
openFDA lists no recalls under a recalling firm named Nanjing Bestview Laser S&T 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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Nanjing Jusha Display Technology Co., Ltd. (26 510(k)s)
- Nanjing Eco Microwave System Co., Ltd. (2 510(k)s)
- Nanjing Jin Bai HE Medical Apparatus Co., Ltd. (2 510(k)s)
- Nanjing Kangni Smart Technology Co., Ltd. (2 510(k)s)
- Nanjing Perlove Medical Equipment Co., Ltd. (2 510(k)s)
- Nanjing Vishee Medical Technology Co., Ltd. (2 510(k)s)
- Nanjing 3h Medical Products Co., Ltd. (1 510(k)s)
- Nanjing CareMoving Rehabilitation Equipment Co.,Ltd (1 510(k)s)
- Nanjing Devin Medical Technology Co., Ltd. (1 510(k)s)
- Nanjing Dewen Medical Technology Co., Ltd. (1 510(k)s)
- Nanjing E-Take Medical Apparatus Co., Ltd. (1 510(k)s)
- Nanjing Jiahe Dental Technology Co., Ltd. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Nanjing Bestview Laser S&T Co., Ltd.?
FDA lists 5 510(k) clearances under the applicant name “Nanjing Bestview Laser S&T Co., Ltd.” (first 2024, latest 2026), 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 Nanjing Bestview Laser S&T Co., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Nanjing Bestview Laser S&T Co., Ltd. is 90 days. Since 2017: 90 days, versus 90 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Nanjing Bestview Laser S&T Co., Ltd.?
The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 4); ONF (Powered Light Based Non-Laser Surgical Instrument With Thermal Effect, 1).
Next steps
- See all 5 Nanjing Bestview Laser S&T Co., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code GEX, Nanjing Bestview Laser S&T 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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.