Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Fibreoptic light cable FDA UDI
- Device Name
- Light Cable, Bifurcated, 90 Degree FDA UDI
- Model / Reference
- AR-3240-5090 FDA UDI
- Description
- Light Cable, Bifurcated, 90 Degree FDA UDI
Identifiers
- Catalog Number
- AR-3240-5090 FDA UDI
- Primary DI / UDI-DI
- 00888867353244 FDA UDI
- 510(k) Number
- K901035 FDA UDI
- FDA Product Code
- FST FDA UDI
- GMDN Term
- Fibreoptic light cable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Fibreoptic light cable
Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fibreoptic light cable.
- JEDMED — JEDMED Instrument Company · Class I
- JEDMED — JEDMED Instrument Company · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Gimmi — Gimmi GmbH · Class II
- ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class II
- JEDMED — JEDMED Instrument Company · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- FENTEX — FENTEX medical GmbH · Class I
Cleared under the same submission
K901035 also covers:
- Arthrex® — Arthrex, Inc.
- Arthrex® — Arthrex, Inc.
- Arthrex® — Arthrex, Inc.
- Arthrex® — Arthrex, Inc.
- Arthrex® — Arthrex, Inc.
- CONMED — Conmed Corporation
- PIPELINE — Depuy Spine, Inc.
- PIPELINE — Depuy Spine, Inc.
- SPOTLIGHT — Depuy Spine, Inc.
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
- Snowden-Pencer — STERIS CORPORATION
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
- Arthrex, Inc.
Sources (1)
- FDA UDI 2b897912-bea4-4424-b84b-9c08a904217e 36 fields · synced Jun 8, 2026