Identity
- Trade Name
- RF Generator FDA UDI
- Generic Name
- Electrosurgical system FDA UDI
- Device Name
- RF Generator FDA UDI
- Model / Reference
- IEC6-IENSP170 FDA UDI
- Description
- RF Generator FDA UDI
Identifiers
- Catalog Number
- IEC6-IENSP170 FDA UDI
- Primary DI / UDI-DI
- 00810026181559 FDA UDI
- 510(k) Number
- K183611 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrosurgical system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Electrosurgical system
RF Generator by Soniquence, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K183611 also covers:
- Dual Footswitch — Soniquence, LLC
- Neutral Plate — Soniquence, LLC
- Neutral Plate — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
- RF Generator — Soniquence, LLC
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
- Soniquence, LLC
Sources (1)
- FDA UDI f3f36170-e37d-496d-8d1a-3568fae3ae8f 35 fields · synced Jun 1, 2026