Data / Medical devices / China / Dezhou Globalipl Medical Technology Co., Ltd.
Dezhou Globalipl Medical Technology Co., Ltd.: FDA-registered device maker in Dezhou Shandong, China, 4 510(k) clearances
Dezhou Globalipl Medical Technology Co., Ltd. is registered with the FDA (registration 3043127589) in Dezhou Shandong, China. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 9, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043127589
- Address
- F-5, Building 1, Mengshan Road, Songguantun Street, Tianqu New District, Dezhou Shandong, China, 253000
- Owner or operator
- Dezhou Globalipl Medical Technology Co., Ltd. (10094671)
- Roles
- Manufacturer
- First device listed
- December 16, 2025
- Registered through
- 2026
- Brand names listed
- CO2 Laser Equipment, IPL + Diode Laser machine, Intense Pulsed Light Equipment, Manufacture Medical Device, Roller Body Shaping Machine-US08F
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 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 |
|---|---|---|---|---|---|---|
| December 9, 2022 | K222916 | US 450 Diode Laser Equipment | GEX | Substantially Equivalent | Beijing Globalipl Development Co., Ltd. | accessdata.fda.gov |
| August 12, 2022 | K220385 | Intense Pulsed Light Equipment | ONF | Substantially Equivalent | Beijing Globalipl Development Co., Ltd. | accessdata.fda.gov |
| February 1, 2022 | K212611 | CO2 Laser Equipment | GEX | Substantially Equivalent | Beijing Globalipl Development Co., Ltd. | accessdata.fda.gov |
| March 25, 2020 | K193328 | IPL + Diode Laser Machine | ONF | Substantially Equivalent | Beijing Globalipl Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Massager, Therapeutic, Electric
Updated December 9, 2022. 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.