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Apollo Light TMS Therapy System
FDA UDIFDA 510(k)Class II (US FDA UDI)
510(k) K260560
Identity
- Trade Name
- Apollo Light TMS Therapy System FDA UDI
- Generic Name
- Magnetic neural stimulation system FDA UDI
- Model / Reference
- 918010 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260526050101 FDA UDI
- FDA Product Code
- OBP FDA UDI
- GMDN Term
- Magnetic neural stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5805 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Magnetic neural stimulation system
Apollo Light TMS Therapy System by MAG & More GmbH — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K260560 | Class II | Active |
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Manufacturer
- Manufacturer
- MAG & More GmbH
Sources (2)
- FDA UDI 5d92b7f2-f420-479c-b465-470561d0fd0e 56 fields · synced Jun 18, 2026
- FDA 510(k) K260560 1 fields · synced Jun 4, 2026