Beijing Sano Laser S&T Development Co.,Ltd: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Beijing Sano Laser S&T Development Co.,Ltd” (first 2020, latest 2026), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 122 days. Since 2017 the median was 122 days, against 93 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

YearClearancesMedian review days
20201257
20210—
20220—
20231245
20241119
20252100
2026193

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Beijing Sano Laser S&T Development Co.,Ltd took a median 122 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 93 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
GEXPowered Laser Surgical Instrument55
NGXStimulator, Muscle, Powered, For Muscle Conditioning11

Review panels

Most recent Beijing Sano Laser S&T Development Co.,Ltd 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K260690LumiGlam Laser System (SHE-LSP601-3)GEX2026-06-0493
K250936Q-Switched Nd:YAG Laser (SHE-LSP101-1)GEX2025-06-1276
K242941CO2 Laser Therapy Systems (SHE-LSP003-1)GEX2025-01-27124
K233416Cryojet Plus (SHE-ACP001-1)GEX2024-02-06119
K230024HI-EMT MAGSHAPENGX2023-09-06245
K191970Diode Laser Hair Removal SystemGEX2020-04-06257

Recalls

openFDA lists no recalls under a recalling firm named Beijing Sano Laser S&T Development 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.

Frequently asked questions

How many FDA 510(k) clearances are listed under Beijing Sano Laser S&T Development Co.,Ltd?

FDA lists 6 510(k) clearances under the applicant name “Beijing Sano Laser S&T Development Co.,Ltd” (first 2020, latest 2026), across 2 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Beijing Sano Laser S&T Development Co.,Ltd?

The median time from FDA receipt to decision across 510(k)s cleared under the name Beijing Sano Laser S&T Development Co.,Ltd is 122 days. Since 2017: 122 days, versus 93 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Beijing Sano Laser S&T Development Co.,Ltd?

The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 5); NGX (Stimulator, Muscle, Powered, For Muscle Conditioning, 1).

Next steps

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.

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