Shenzhen Fansizhe Science and Technology Co., Ltd.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Shenzhen Fansizhe Science and Technology Co., Ltd.” (first 2022, latest 2025), across 1 product code in 1 review panel. Median 510(k) review time under this name: 88 days. Since 2017 the median was 88 days, against 82 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
20222122
2023188
20240—
2025257
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Shenzhen Fansizhe Science and Technology Co., Ltd. took a median 88 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 82 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
OHTLight Based Over-The-Counter Hair Removal55

Review panels

Most recent Shenzhen Fansizhe Science and Technology Co., Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K253881Intense Pulsed Light (IPL) System (Models: T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T505KQ, T505KH, T505KF, SL-B505WM)OHT2025-12-2925
K251173Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF)OHT2025-07-1489
K223928Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016KOHT2023-03-2888
K221569Intense Pulsed Light (IPL) System, model: T013C, T015C, T015KOHT2022-06-3030
K212881Intense Pulsed Light (IPL) SystemOHT2022-04-11213

Recalls

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

FDA lists 5 510(k) clearances under the applicant name “Shenzhen Fansizhe Science and Technology Co., Ltd.” (first 2022, latest 2025), across 1 product code 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 Fansizhe Science and Technology Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Fansizhe Science and Technology Co., Ltd. is 88 days. Since 2017: 88 days, versus 82 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Shenzhen Fansizhe Science and Technology Co., Ltd.?

The most frequent FDA product codes under this applicant name are OHT (Light Based Over-The-Counter Hair Removal, 5).

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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