Identity
- Trade Name
- Senhance FDA UDI
- Generic Name
- Robotic electrosurgical instrument, monopolar, reusable FDA UDI
- Device Name
- Monopolar L-Hook Electrode, Long FDA UDI
- Model / Reference
- X0007036 FDA UDI
- Description
- Monopolar L-Hook Electrode, Long FDA UDI
Identifiers
- Catalog Number
- 210-11038 FDA UDI
- Primary DI / UDI-DI
- 00815440020231 FDA UDI
- 510(k) Number
- K171120 FDA UDI
- FDA Product Code
- NAY FDA UDI
- GMDN Term
- Robotic electrosurgical instrument, monopolar, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 410 Millimeter FDA UDIOuter Diameter — 5 Millimeter FDA UDI
Category: Robotic electrosurgical instrument, monopolar, reusable
Senhance by Asensus Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Robotic electrosurgical instrument, monopolar, reusable.
- EndoWrist — Intuitive Surgical, Inc. · Class II
- EndoWrist;daVinci Si — Intuitive Surgical, Inc. · Class II
- Single-Site; daVinci Si — Intuitive Surgical, Inc. · Class II
- EndoWrist;daVinci Si — Intuitive Surgical, Inc. · Class II
- EndoWrist;daVinci Si — Intuitive Surgical, Inc. · Class II
- EndoWrist SP — Intuitive Surgical, Inc. · Class II
- EndoWrist — Intuitive Surgical, Inc. · Class II
- EndoWrist SP — Intuitive Surgical, Inc. · Class II
Cleared under the same submission
K171120 also covers:
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
- Senhance — Asensus Surgical, Inc.
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
- Asensus Surgical, Inc.
Sources (1)
- FDA UDI 387f3ea8-859d-475d-98c1-1714584df352 36 fields · synced Sep 18, 2026