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Sign in to claim this brandRelievant Medsystems, Inc.
United States·US-MF-000030056
Last updated June 8, 2026
Information
- Country
- United States
- Address
- 1230, Midas Way, Sunnyvale, California, United States
- Website
- bsci.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Kay Adair
- EUDAMED SRN
- US-MF-000030056
- FDA FEI Number
- —
- DUNS Number
- 099324362
Catalogue (29)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Intracept | RLV 0075 | FDA UDI | Class II | Active |
| Intracept | RLV 0035 | FDA UDI | Class II | Active |
| Intracept RF Probe | RLV 0015 | FDA UDI | Class II | Unknown |
| Intracept | RLV 0055 | FDA UDI | Class II | Active |
| Intracept | FG 0038 | FDA UDI | Class II | Unknown |
| Intracept | FG 0046 | FDA UDI | Class II | Unknown |
| Intracept | FG 0060 | FDA UDI | Class II | Unknown |
| Intracept | RLV0065 | FDA UDI | Class II | Active |
| Intracept | RLV 0045 | FDA UDI | Class II | Active |
| Intracept | FG 0043 | FDA UDI | Class II | Unknown |
| Intracept | RLV PK | FDA UDI | Class II | Unknown |
| Intracept | RLV PKBLR | FDA UDI | Class II | Unknown |
| Intracept | RLV PKTLR | FDA UDI | Class II | Unknown |
| Relievant | FG 0052 | FDA UDI | Class II | Active |
| Intracept | FG 0054 | FDA UDI | Class II | Unknown |
| Relievant | FG 0052 | FDA UDI | Class II | Active |
| Intracept | FG 0045 | FDA UDI | Class II | Unknown |
| Intracept | RLV 0020 | FDA UDI | Class II | Active |
| Intracept RF Probe | RLV 0015 | FDA UDI | Class II | Active |
| Intracept Flexible Bi-Polar Rf Probe And Easy Access Instrument Set, Model Fg0018 (probe), Fg0036 (instrument Set) | K100641 | FDA 510(k) | Class II | Active |
| Intracept Intraosseous Nerve Ablation System | K213836 | FDA 510(k) | Class II | Active |
| Intracept Flexible Bi-Polar Rf Probe And Curved Instrument Set, Models: Fg0018, Fg0026 | K083856 | FDA 510(k) | Class II | Active |
| Relievant Medsystems RF Generator | K171143 | FDA 510(k) | Class II | Active |
| Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator | K190504 | FDA 510(k) | Class II | Active |
| Intracept Intraosseous Nerve Ablation System | K222281 | FDA 510(k) | Class II | Active |
| INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set | K153272 | FDA 510(k) | Class II | Active |
| INTRACEPT Intraosseous Nerve Ablation System | K170827 | FDA 510(k) | Class II | Active |
| Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe) | K180369 | FDA 510(k) | Class II | Active |
| Intracept Bi-Polar Rf Probe, Model 04814 | K070443 | FDA 510(k) | Class II | Active |
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