Data / Medical devices / United States / XOD Inc
XOD Inc: FDA-registered device maker in Philadelphia, PA, United States, 2 510(k) clearances
XOD Inc is registered with the FDA (registration 3030420005) in Philadelphia, PA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 27, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3030420005
- Address
- 3245 Amber St, Philadelphia, PA, United States, 19134
- Owner or operator
- Manifest Aesthetics Inc (10089997)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- January 31, 2024
- Registered through
- 2026
- Brand names listed
- Breeze, Wonder Touch
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Specification developer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Specification developer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| February 27, 2025 | K242175 | XOD Diathermia Radiofrequency Device | PBX | Substantially Equivalent | Xod, Inc. | accessdata.fda.gov |
| February 23, 2021 | K203804 | Global Med Systems Milesman Compact Laser | GEX | Substantially Equivalent | Global Med Systems SL | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
- All makers of Powered Laser Surgical Instrument
- All makers of Brush, Dermabrasion, Powered
Updated February 27, 2025. 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.