Data / Medical devices / China / Beijing Globalipl Development Co., Ltd.
Beijing Globalipl Development Co., Ltd.: FDA-registered device maker in Beijing, China, 4 510(k) clearances
Beijing Globalipl Development Co., Ltd. is registered with the FDA (registration 3012799115) in Beijing, China. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 9, 2022. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3012799115
- Address
- F-8 Qunyinghui Building, Jinyuan Rd.32, Daxing Economic Development Zone, Beijing, China, 102628
- Owner or operator
- Beijing Globalipl Development Co., Ltd. (10075244)
- Roles
- Specification developer
- First device listed
- June 10, 2020
- Registered through
- 2027
- Brand names listed
- CO2 Laser Equipment, Diode Laser Equipment, IPL + Diode Laser machine, Intense Pulsed Light Equipment, Roller Body Shaping Machine-US08F, Zemits DuoCratus, model:Alby pro, model:Aphro prime
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Specification developer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Specification developer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Specification developer | 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 Powered Laser Surgical Instrument
- All makers of Lamp, Infrared, Therapeutic Heating
- 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.