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Sign in to claim this brandMedrobotics Corporation
US
Last updated May 23, 2026
Information
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- 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 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flex | 50226PKG | FDA UDI | Class I | Active |
| Flex | 50152 | FDA UDI | Class I | Active |
| Flex | 50710PKG | FDA UDI | Class I | Active |
| Flex | 50225PKG | FDA UDI | Class I | Active |
| Flex | 50204PKG | FDA UDI | Class I | Active |
| Flex | 26570 | FDA UDI | Class I | Active |
| Flex | 25331 | FDA UDI | Class II | Active |
| Flex | 25178 | FDA UDI | Class II | Active |
| Flex | Instrument Assembly part | FDA UDI | Class II | Active |
| Flex | 50642 | FDA UDI | Class II | Active |
| Flex | 50111PKG | FDA UDI | Class I | Active |
| Flex | 26114 | FDA UDI | Class II | Active |
| Flex | 50420 | FDA UDI | Class II | Active |
| Flex | 50125PKG | FDA UDI | Class I | Active |
| Flex | 50083 | FDA UDI | Class II | Active |
| Flex | 50224PKG | FDA UDI | Class I | Active |
| Flex | 22995 | FDA UDI | Class II | Active |
| Flex | 25777 | FDA UDI | Class II | Active |
| Flex | 50641 | FDA UDI | Class II | Active |
| Flex | 25332 | FDA UDI | Class II | Active |
| Flex | 50937 | FDA UDI | Class II | Active |
| Flex | 50207PKG | FDA UDI | Class I | Active |
| Flex | 24698 | FDA UDI | Class II | Active |
| Flex | 25329 | FDA UDI | Class II | Active |
| Flex | 50474 | FDA UDI | Class II | Active |
| Flex | 50079 | FDA UDI | Class II | Active |
| Flex | 50127PKG | FDA UDI | Class I | Active |
| Medrobotics Flex Robotic System | K170453 | FDA 510(k) | Class II | Active |
| Flex Robotic System and Flex Colorectal Drive | K162330 | FDA 510(k) | Class II | Active |
| Medrobotics Flex System | K150776 | FDA 510(k) | Class II | Active |
| Flex Robotic System and Flex Transabdominal Drive | K172796 | FDA 510(k) | Class II | Active |
| Medrobotics Flex Robotic System | K172036 | FDA 510(k) | Class II | Active |
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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. |