Identity
- Trade Name
- LITe DECOMPRESSION FDA UDI
- Generic Name
- Surgical instrument fibreoptic light FDA UDI
- Device Name
- LIGHT CABLE FDA UDI
- Model / Reference
- 48089999 FDA UDI
- Description
- LIGHT CABLE FDA UDI
Identifiers
- Catalog Number
- 48089999 FDA UDI
- Primary DI / UDI-DI
- 07613327064926 FDA UDI
- 510(k) Number
- K122637 FDA UDI
- FDA Product Code
- FST FDA UDI
- GMDN Term
- Surgical instrument fibreoptic light 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
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
Yes
FDA UDI
Category: Surgical instrument fibreoptic light
LITe DECOMPRESSION by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical instrument fibreoptic light.
- Camber Spine OLIF Surgical Illuminator — LUMITEX, INC. · Class I
- Precision Spine Midline Cortical Surgical Illuminator — LUMITEX, INC. · Class I
- Novus N-Sight Disposable Surgical Light — LUMITEX, INC. · Class I
- Altus Spine ACMI Fiber Optic Cable — LUMITEX, INC. · Class I
- CoreLink Bifurcated Illuminator — LUMITEX, INC. · Class I
- Pinnacle Spine Products Surgical Illuminator — LUMITEX, INC. · Class I
- Fiber Optic Light Cable — GULF FIBEROPTICS, INC. · Class I
- Fiber Optic Light Cable — GULF FIBEROPTICS, INC. · Class I
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
- Stryker Corp.
Sources (1)
- FDA UDI f2fd22da-7690-44e0-a25b-ff620bf18d7f 35 fields · synced May 30, 2026