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Sign in to claim this brandMedrobotics Corporation
US
Last updated May 23, 2026
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 002764627
Catalogue (82)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flex | 25386 | FDA UDI | Class II | Active |
| Flex | 24324-L | FDA UDI | Class II | Active |
| Flex | 50124PKG | FDA UDI | Class I | Active |
| Flex | 50208PKG | FDA UDI | Class I | Active |
| Flex | 25776 | FDA UDI | Class II | Active |
| Flex | 25171 | FDA UDI | Class II | Active |
| Flex | 50644 | FDA UDI | Class II | Active |
| Flex | 23392 | FDA UDI | Class II | Active |
| Flex | 50640 | FDA UDI | Class II | Active |
| Flex | 24699 | FDA UDI | Class II | Active |
| Flex | 50128PKG | FDA UDI | Class I | Active |
| Flex | 26470 | FDA UDI | Class II | Active |
| Flex | 50137PKG | FDA UDI | Class I | Active |
| Flex | 25463 | FDA UDI | Class II | Active |
| Flex | 25171 | FDA UDI | Class II | Active |
| Flex | 26473 | FDA UDI | Class II | Active |
| Flex | 25327 | FDA UDI | Class II | Active |
| Flex | 50149PKG | FDA UDI | Class I | Active |
| Flex | 51075 | FDA UDI | Class II | Active |
| Flex | 23157 | FDA UDI | Class II | Active |
| Flex | Instrument Assembly part | FDA UDI | Class II | Active |
| Flex | 50639 | FDA UDI | Class II | Active |
| Flex | 50421 | FDA UDI | Class II | Active |
| Flex | 50129PKG | FDA UDI | Class I | Active |
| Flex | 50134PKG | FDA UDI | Class I | Active |
| Flex | 26471 | FDA UDI | Class II | Active |
| Flex | 50419 | FDA UDI | Class II | Active |
| Flex | 25171 | FDA UDI | Class II | Active |
| Flex | 50951 | FDA UDI | Class I | Active |
| Flex | 50126PKG | FDA UDI | Class I | Active |
| Flex | 50074PKG | FDA UDI | Class I | Active |
| Flex | 25171 | FDA UDI | Class II | Active |
| Flex | 23498 | FDA UDI | Class II | Active |
| Flex | 50206PKG | FDA UDI | Class I | Active |
| Flex | 24324 | FDA UDI | Class II | Active |
| Flex | 26472 | FDA UDI | Class II | Active |
| Flex | 50418 | FDA UDI | Class II | Active |
| Flex | 25330 | FDA UDI | Class II | Active |
| Flex | 50709PKG | FDA UDI | Class I | Active |
| Flex | 25778 | FDA UDI | Class II | Active |
| Flex | 50203PKG | FDA UDI | Class I | Active |
| Flex | 25328 | FDA UDI | Class II | Active |
| Flex | 25171 | FDA UDI | Class II | Active |
| Flex | 25173 | FDA UDI | Class II | Active |
| Flex | 25597 | FDA UDI | Class II | Active |
| Flex | 50220PKG | FDA UDI | Class I | Active |
| Flex | 50123PKG | FDA UDI | Class I | Active |
| Flex | 50931 | FDA UDI | Class II | Active |
| Flex | 50147PKG | FDA UDI | Class I | Active |
| Flex | 50205PKG | FDA UDI | Class I | Active |
Related Companies
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jan 25, 2019 | Z-1192-2019 | — | terminated | The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators. |
| Jan 25, 2019 | Z-1191-2019 | — | terminated | The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators. |