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

FDA lists 6 510(k) clearances under the applicant name “Shenzhen Desida Technology Co., Ltd.” (first 2022, latest 2026), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 94 days. Since 2017 the median was 94 days, against 87 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
20222112
20230—
20241100
2025282
2026188

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Shenzhen Desida Technology 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 87 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
BTAPump, Portable, Aspiration (Manual Or Powered)33
OHTLight Based Over-The-Counter Hair Removal22
OHSLight Based Over The Counter Wrinkle Reduction11

Review panels

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

510(k)DeviceProduct codeDecision dateReview days
K254079LED Light Therapy Mask (Models: T2, RLD10)OHS2026-03-1688
K251450Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009)BTA2025-06-0628
K244033Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)BTA2025-05-16137
K233901Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009)BTA2024-03-20100
K221643Hair Removal Device (Model: IPL-D26, IPL-D19)OHT2022-10-21137
K221635IPL sapphire ice cooling hair remove deviceOHT2022-08-3186

Recalls

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

FDA lists 6 510(k) clearances under the applicant name “Shenzhen Desida Technology Co., Ltd.” (first 2022, latest 2026), across 3 product codes 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 Shenzhen Desida Technology Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Desida Technology Co., Ltd. is 94 days. Since 2017: 94 days, versus 87 days for all cleared 510(k)s in the same product codes.

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

The most frequent FDA product codes under this applicant name are BTA (Pump, Portable, Aspiration (Manual Or Powered), 3); OHT (Light Based Over-The-Counter Hair Removal, 2); OHS (Light Based Over The Counter Wrinkle Reduction, 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 (spelling variants such as punctuation and legal suffixes combined); 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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