Data / Medical devices / United States / Velabody LLC
Velabody LLC: FDA-registered device maker in Hollywood, FL, United States, 5 510(k) clearances
Velabody LLC is registered with the FDA (registration 3034995492) in Hollywood, FL, United States. It lists 5 device types. The FDA files 5 510(k) clearances under its listings, the newest dated December 20, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034995492
- Address
- 3800 S Ocean DR, Ste G5-D, Hollywood, FL, United States, 33019
- Owner or operator
- VELABODY LLC (10092345)
- Roles
- Repackager or relabeler
- First device listed
- February 17, 2025
- Registered through
- 2026
- Brand names listed
- Aqua Facial, Diode Laser Therapy System, Fractional CO2 Laser Therapy System (FG900-S,FG900-S2,PhantomClear), Intensity Pulsed Light Therapy System, ND YAG Q-Switch Laser Therapy Machine FG2010 FG2010-B FG2014, Slimming Treatment Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Vacuum, Light Induced Heating | NUV | 2 | Repackager or relabeler | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Repackager or relabeler | 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 20, 2024 | K241670 | Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2) | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| March 15, 2024 | K233307 | Intensity Pulsed Light Therapy System | ONF | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| February 20, 2024 | K231896 | Diode Laser Therapy System | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| March 2, 2017 | K161892 | Slimming Treatment Device | NUV | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
| February 22, 2017 | K161926 | ND YAG Q-switch Laser Therapy Machine | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- 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
- All makers of Massager, Vacuum, Light Induced Heating
- All makers of Brush, Dermabrasion, Powered
Updated December 20, 2024. 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.