Identity
- Trade Name
- 10THERMA FDA UDI
- Generic Name
- Electrosurgical system FDA UDI
- Device Name
- 10THERMA Handpiece FDA UDI
- Model / Reference
- TMHP02 FDA UDI
- Description
- 10THERMA Handpiece FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809709380350 FDA UDI
- 510(k) Number
- K232992 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
Category: Electrosurgical system
10therma by Tentech Co. , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K232992 also covers:
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
- Tentech Co. , Ltd.
Sources (1)
- FDA UDI 0f0f4c2a-0c70-48fb-8f2f-722c739006a3 34 fields · synced May 30, 2026