Identity
- Trade Name
- DYONICS RF, HOOK FDA UDI
- Generic Name
- Endoscopic surgical probe FDA UDI
- Device Name
- DYONICS RF HOOK 30 DEG FDA UDI
- Model / Reference
- 72202145 FDA UDI
- Description
- DYONICS RF HOOK 30 DEG FDA UDI
Identifiers
- Catalog Number
- 72202145 FDA UDI
- Primary DI / UDI-DI
- 03596010625076 FDA UDI
- 510(k) Number
- K093165 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Endoscopic surgical probe 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endoscopic surgical probe
Dyonics Rf, Hook by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic surgical probe.
- Tecomet — Tecomet,Inc · Class I
- ENDOTRAC — Stryker Corp. · Class II
- MAGNETIC PROBE — SONTEC INSTRUMENTS, INC. · Class I
- Tecomet — Tecomet,Inc · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
- Lightning — RESPONSIVE ORTHOPEDICS LLC · Class I
- Rasp Probe — Biomet Orthopedics, Inc. · Class I
Cleared under the same submission
K093165 also covers:
- DYONICS RF — Smith & Nephew, Inc.
- DYONICS RF — Smith & Nephew, Inc.
- DYONICS RF, ABLATION — Smith & Nephew, Inc.
- DYONICS RF, BROADNOSE — Smith & Nephew, Inc.
- DYONICS RF, CROSS — Smith & Nephew, Inc.
- DYONICS RF, CURVE — Smith & Nephew, Inc.
- DYONICS RF, DYNAMO — Smith & Nephew, Inc.
- DYONICS RF, HEDGEHOG — Smith & Nephew, Inc.
- DYONICS RF, ROUND — Smith & Nephew, Inc.
- DYONICS RF, SLICE — Smith & Nephew, Inc.
- DYONICS RF, WHIRLWIND — Smith & Nephew, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 3f2dd825-0a75-48e9-b86f-8c8d2dae8867 36 fields · synced Jun 6, 2026