Identity
- Trade Name
- Cyberwand USL Wrench FDA UDI
- Generic Name
- Surgical torque wrench, reusable FDA UDI
- Model / Reference
- CW-USLW FDA UDI
Identifiers
- Primary DI / UDI-DI
- H891CWUSLW2 FDA UDI
- 510(k) Number
- K120303 FDA UDI
- FDA Product Code
- FFK FDA UDI
- GMDN Term
- Surgical torque wrench, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4480 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical torque wrench, reusable
Cyberwand USL Wrench by Cybersonics Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BIONNOVATION — BIONNOVATION PRODUTOS BIOMEDICOS LTDA. · Class I
Cleared under the same submission
K120303 also covers:
- CyberWand Probe Set — CYBERSONICS INC
- CyberWand USL Advanced Transducer — CYBERSONICS INC
- CyberWand USL Foot Switch — CYBERSONICS INC
- CyberWand USL Generator — CYBERSONICS INC
- CyberWand USL NoseCone Kit — CYBERSONICS INC
- CyberWand USL Power Cord — CYBERSONICS INC
- CyberWand USL Ultrasonic Lithotripsy System — CYBERSONICS INC
- CYBERWAND — Gyrus Acmi, 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
- Cybersonics Inc
Sources (1)
- FDA UDI 7dfd9a40-7a0d-4abf-9ec4-84493a84b3cf 33 fields · synced May 30, 2026