← Back to catalogue

Fiberoptics Technology Inc

FDA UDI

Class II (US FDA UDI)

by Fiberoptics Technology, Inc.

Identity

Trade Name
Fiberoptics Technology Inc FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
LO-50 LED Fiber Optic Light Source FDA UDI
Model / Reference
LO-50 FDA UDI
Description
LO-50 LED Fiber Optic Light Source FDA UDI

Identifiers

Primary DI / UDI-DI
00862658000302 FDA UDI
FDA Product Code
FCW FDA UDI
NTN FDA UDI
GMDN Term
Operating room light FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating room light

Fiberoptics Technology Inc by Fiberoptics Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fiberoptics Technology, Inc.

Sources (1)

  • FDA UDI e17e1528-0035-4e50-91cc-521e9161219e 33 fields · synced Jun 7, 2026