Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Shenzhen Qianyu Technology Co., Ltd. — Predicate Candidate Screening

7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

79 daysmedian FDA review time
263 days90th percentile
7clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K261851LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Shenzhen Qianyu Technology Co., Ltd.2026-08-04620
K250227JOVS Electric Stimulation Beauty Device (JE2)Shenzhen Qianyu Technology Co., Ltd.2025-10-172630
K244020Wrinkle Treatment Device (JM1, JM2B)Shenzhen Qianyu Technology Co., Ltd.2025-05-011250
K240360Wrinkle Treatment Device (JM2)Shenzhen Qianyu Technology Co., Ltd.2024-04-05590
K231800IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9Shenzhen Qianyu Technology Co., Ltd.2023-09-07790
K220645Hand-held IPL device (JOVS Hair Removal Device)Shenzhen Qianyu Technology Co., Ltd.2022-04-27540
K214113Hand-held IPL device(JOVS Graphene Hair Removal Device)Shenzhen Qianyu Technology Co., Ltd.2022-03-28880

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda