Beijing Nubway S&T Co., Ltd.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Beijing Nubway S&T Co., Ltd.” (first 2025, latest 2026), across 1 product code in 1 review panel. Median 510(k) review time under this name: 94 days. Since 2017 the median was 94 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 |
|---|---|---|
| 2025 | 2 | 187 |
| 2026 | 4 | 62 |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Beijing Nubway S&T Co., Ltd. took a median 94 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 | 6 | 6 |
Review panels
Most recent Beijing Nubway S&T Co., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K261673 | LED Therapy Device (QLXY-01) | GEX | 2026-09-17 | 119 |
| K261841 | Q Switched Nd:YAG Laser machine (QLQW-01) | GEX | 2026-08-11 | 69 |
| K261693 | Diode laser hair removal machine (QDTM-04) | GEX | 2026-07-17 | 56 |
| K261674 | Skin Air Cooling System (QALF-01) | GEX | 2026-07-16 | 56 |
| K242951 | Diode laser hair removal machine (QDTM-02) | GEX | 2025-04-28 | 215 |
| K242943 | Q Switched Nd:YAG Laser machine (QNHF-01) | GEX | 2025-03-03 | 159 |
Recalls
openFDA lists no recalls under a recalling firm named Beijing Nubway 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.
- Beijing Choice Electronic Technololgy Co., Ltd. (29 510(k)s)
- Beijing Choice Electronic Technology Co., Ltd. (14 510(k)s)
- Beijing Adss Development Co., Ltd. (10 510(k)s)
- Beijing Biosis Healing Biolog Ical Technology Co., Ltd. (7 510(k)s)
- Beijing East Whale Imaging Technology Co., Ltd. (6 510(k)s)
- Beijing Sano Laser S&T Development Co.,Ltd (6 510(k)s)
- Beijing Zksk Technology Co., Ltd. (6 510(k)s)
- Beijing Honkon Technologies Co., Ltd. (5 510(k)s)
- Beijing Superlaser Technology Co., Ltd. (5 510(k)s)
- Beijing Demax Medical Technology Co.,Ltd (4 510(k)s)
- Beijing Fule Science & Technology Development Co., Ltd. (4 510(k)s)
- Beijing Globalipl Development Co., Ltd. (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Beijing Nubway S&T Co., Ltd.?
FDA lists 6 510(k) clearances under the applicant name “Beijing Nubway S&T Co., Ltd.” (first 2025, latest 2026), across 1 product code 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 Beijing Nubway S&T Co., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Beijing Nubway S&T Co., Ltd. is 94 days. Since 2017: 94 days, versus 90 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Beijing Nubway S&T Co., Ltd.?
The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 6).
Next steps
- See all 6 Beijing Nubway S&T Co., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code GEX, Beijing Nubway 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.