Shenzhen Fansizhe Science and Technology Co., Ltd.
Shenzhen Guangdong, CN
SHENZHEN FANSIZHE SCIENCE AND TECHNOLOGY CO., LTD. appears in FDA device records in Shenzhen Guangdong, CN. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Shenzhen Fansizhe Science and Technology Co., Ltd. between 2022 and 2025. The busiest year on record is 2022, with 2. The most recent is 2025, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2022 | 2 |
| 2023 | 1 |
| 2025 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K253881 | Intense Pulsed Light (IPL) System (Models: T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T505KQ, T505KH, T505KF, SL-B505WM) | OHT | Substantially Equivalent | |
| K251173 | Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF) | OHT | Substantially Equivalent | |
| K223928 | Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K | OHT | Substantially Equivalent | |
| K221569 | Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K | OHT | Substantially Equivalent | |
| K212881 | Intense Pulsed Light (IPL) System | OHT | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3023281259 | 3023281259 | SHENZHEN FANSIZHE SCIENCE AND TECHNOLOGY CO., LTD. | 2nd, 3rd And 4th floors, No.11, Henggangxia Industrial Zone, Shenzhen Guangdong 518125 CN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain