Identity
- Trade Name
- Apollo Knee FDA UDI
- Generic Name
- Robotic surgical arm system FDA UDI
- Device Name
- Camera Assembly VT FDA UDI
- Model / Reference
- COR.TS.0005 FDA UDI
- Description
- Camera Assembly VT FDA UDI
Identifiers
- Catalog Number
- COR.TS.0005 FDA UDI
- Primary DI / UDI-DI
- 05056139246012 FDA UDI
- 510(k) Number
- K231172 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Robotic surgical arm system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 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
No
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: Robotic surgical arm system
Apollo Knee by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Robotic surgical arm system.
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- Flex — Medrobotics Corporation · Class II
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- FLEX — Medrobotics Corporation · Class II
- Senhance — Asensus Surgical, Inc. · Class II
- ARTAS System — Venus Concept Inc. · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Corin Ltd
Sources (1)
- FDA UDI 8891c3f0-51ec-4220-b630-1c7719585caa 36 fields · synced May 30, 2026