Data / Medical devices / China / Wuhan Phomed Technology Co., Ltd.
Wuhan Phomed Technology Co., Ltd.: FDA-registered device maker in Wuhan Hubei, China, 2 510(k) clearances
Wuhan Phomed Technology Co., Ltd. is registered with the FDA (registration 3026939957) in Wuhan Hubei, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 8, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026939957
- Address
- Room 02, 3F, Building 2, Gezhouba Sun City, No. 40 Gaoxin 4th Road East Lake New Technology Development Zone, Wuhan Hubei, China, 430000
- Owner or operator
- Wuhan Phomed Technology Co., Ltd. (10087730)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 31, 2023
- Registered through
- 2026
- Brand names listed
- ATPMAX Laser System ATPmax XDS, ATPMAX Laser System ATPmax XPS, ATPMAX Laser System ATPmax XTS, CURELIGHT Therapy Laser Family CureLight F3-AB30 (aka Aspen Laser Systems Model ASCENT), CURELIGHT Therapy Laser Family CureLight F4-ABCR45, CURELIGHT Therapy Laser Family CureLight F4-ABDR45, CURELIGHT Therapy Laser Family CureLight F4-ACDR45, CureLight F2-A15 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis | PDZ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 8, 2026 | K262346 | CureLight Medical Diode Laser Systems (S3-BF45);CureLight Medical Diode Laser Systems (S2-B30);CureLight Medical Diode Laser Systems (S3-BF30);CureLight Medical Diode Laser Systems (S2-F15);CureLight Medical Diode Laser Systems (S2-H7.5) | GEX | Substantially Equivalent | Wuhan Phomed Technology Co., Ltd. | accessdata.fda.gov |
| March 19, 2026 | K253965 | CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.) | ILY | Substantially Equivalent | Wuhan PHOMED Technology Company , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
Updated October 8, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.