Data / Medical devices / United States / Adp Health Limited
Adp Health Limited: FDA-registered device maker in Norcross, GA, United States, 6 510(k) clearances
Adp Health Limited is registered with the FDA (registration 3030597665) in Norcross, GA, United States. It lists 3 device types. The FDA files 6 510(k) clearances under its listings, the newest dated July 28, 2025. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3030597665
- Address
- 5555 Oakbrook Pkwy Suite 340, Norcross, GA, United States, 30093
- Owner or operator
- ADP Health Limited (10090177)
- Roles
- Repackager or relabeler
- First device listed
- September 25, 2024
- Registered through
- 2026
- Brand names listed
- AVCOO, 3 in 1 TENS UNIT, model TC1241, AVCOO, 3 in 1 TENS UNIT, model TC2241, AVCOO, 3 in 1 TENS UNIT, model TS2301, AVCOO, 3 in 1 TENS UNIT, model TS2321, AVCOO, Adhesive Electrodes, model EB2010, AVCOO, Adhesive Electrodes, model EB2720, AVCOO, Adhesive Electrodes, model EB2M20, AVCOO, OTC TENS & EMS Unit, model TA2224C and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 |
|---|---|---|---|---|---|---|
| July 28, 2025 | K251187 | 3 in 1 TENS UNIT (TC1241, TC2241, TS1241) | NUH | Substantially Equivalent | Changsha Anxiang Medical Technology Co., Ltd. | accessdata.fda.gov |
| June 13, 2025 | K250759 | 3 in 1 TENS UNIT | NGX | Substantially Equivalent | Changsha Anxiang Medical Technology Co., Ltd. | accessdata.fda.gov |
| May 11, 2025 | K250360 | TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) | NUH | Substantially Equivalent | Shenzhen Jiantuo Electronics Co., Ltd. | accessdata.fda.gov |
| February 10, 2025 | K243511 | OTC TENS & EMS Unit | NGX | Substantially Equivalent | Changsha Anxiang Medical Technology Co., Ltd. | accessdata.fda.gov |
| April 10, 2023 | K230164 | TENS and EMS Stimulation (OTC) | NUH | Substantially Equivalent | Changsha Yuwen Medical Equipment Co., Ltd. | accessdata.fda.gov |
| August 11, 2016 | K160138 | Adhesive Electrodes | GXY | Substantially Equivalent | Gmdasz Manufacturing Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Electrode, Cutaneous
Updated July 28, 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.