Facility
Z TECHNOLOGIES, LLC
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 1000511278 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | 2615 WOODACRES RD. ATLANTA, GA, US 30345 |
| Registration status | Active · expires 2026 |
| Parent company | Z TECHNOLOGIES, LLC (owner-operator 9023506) |
| Brand names | ZTEK |
Devices registered here (1)
- Stimulator, Nerve, Transcutaneous, For Pain ReliefProduct code GZJ · Class II · Neurology · 21 CFR 882.5890
Recalls & enforcement
- Class IIOngoing2024-12-02Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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