Shenzhen Qianyu Technology Co., Ltd.: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Shenzhen Qianyu Technology Co., Ltd.” (first 2022, latest 2026), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 79 days. Since 2017 the median was 79 days, against 88 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
2022271
2023179
2024159
20252194
2026162

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Shenzhen Qianyu Technology Co., Ltd. took a median 79 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 88 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
OHSLight Based Over The Counter Wrinkle Reduction33
OHTLight Based Over-The-Counter Hair Removal33
NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes11

Review panels

Most recent Shenzhen Qianyu Technology Co., Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K261851LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED Light Therapy Mask (JML5, JML5+JML7); LED Light Therapy Mask (JML6, JML6+JML8); LED Light Therapy Mask ( JML9, JML9+JML10)OHS2026-08-0462
K250227JOVS Electric Stimulation Beauty Device (JE2)NFO2025-10-17263
K244020Wrinkle Treatment Device (JM1, JM2B)OHS2025-05-01125
K240360Wrinkle Treatment Device (JM2)OHS2024-04-0559
K231800IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9OHT2023-09-0779
K220645Hand-held IPL device (JOVS Hair Removal Device)OHT2022-04-2754
K214113Hand-held IPL device(JOVS Graphene Hair Removal Device)OHT2022-03-2888

Recalls

openFDA lists no recalls under a recalling firm named Shenzhen Qianyu Technology 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 Shenzhen Qianyu Technology Co., Ltd.?

FDA lists 7 510(k) clearances under the applicant name “Shenzhen Qianyu Technology Co., Ltd.” (first 2022, latest 2026), across 3 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 Shenzhen Qianyu Technology Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Qianyu Technology Co., Ltd. is 79 days. Since 2017: 79 days, versus 88 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Shenzhen Qianyu Technology Co., Ltd.?

The most frequent FDA product codes under this applicant name are OHS (Light Based Over The Counter Wrinkle Reduction, 3); OHT (Light Based Over-The-Counter Hair Removal, 3); NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes, 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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