ApexRF Applicator AG614409A
ApexRF Applicator AG614409A is a Class II device made by Inmode MD, Ltd., cleared under FDA 510(k) K210492 on 12 Jul 2021 and listed in FDA GUDID since 4 Jun 2025 (UDI-DI 07290019863359), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07290019863359 | Date4 Jun 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210492 | Date12 Jul 2021 | StatusActive |
Official records
- AccessGUDID record 07290019863359
- FDA 510(k) database K210492
Across registries
- FDA 510(k) K210492 decided 12 Jul 2021 Active
- FDA GUDID UDI-DI 07290019863359 listed 4 Jun 2025 Listed
Timeline
- Cleared FDA 510(k) K210492
- Listed FDA GUDID 07290019863359
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ApexRF Applicator
- Generic name
- Percutaneous radio-frequency ablation system generator
- Model / Ref / Catalog
- AG614409A
- Primary DI / UDI-DI
- 07290019863359
- 510(k) Number
- FDA product code
- GEI, PBX, ISA, NUV
- GMDN term
- Percutaneous radio-frequency ablation system generator
- Device class
- Class II
- Regulation number
- 878.4400, 890.5660, 878.4810
- GUDID distribution status
- In Commercial Distribution
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