Atlas FDA

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

Shenzhen Desida Technology Co., Ltd. · Predicate Candidate Screening

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

100 daysmedian FDA review time
137 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254079LED Light Therapy Mask (Models: T2, RLD10)Shenzhen Desida Technology Co., Ltd.2026-03-16880
K251450Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Shenzhen Desida Technology Co., Ltd.2025-06-06280
K244033Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NAShenzhen Desida Technology Co., Ltd.2025-05-161370
K233901Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA0Shenzhen Desida Technology Co., Ltd.2024-03-201000
K221643Hair Removal Device (Model: IPL-D26, IPL-D19)Shenzhen Desida Technology Co., Ltd.2022-10-211370
K221635IPL sapphire ice cooling hair remove deviceShenzhen Desida Technology Co., Ltd.2022-08-31860

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