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Lucent

FDA UDI

Class II (US FDA UDI)

by Spinal Elements, Inc.

Identity

Trade Name
LUCENT FDA UDI
Generic Name
Fibreoptic operating light system FDA UDI
Device Name
Lucent L Retractor Light, 180mm FDA UDI
Model / Reference
81038-180 FDA UDI
Description
Lucent L Retractor Light, 180mm FDA UDI

Identifiers

Primary DI / UDI-DI
00840606114981 FDA UDI
FDA Product Code
FST FDA UDI
GMDN Term
Fibreoptic operating light system 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic operating light system

Lucent by Spinal Elements, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic operating light system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spinal Elements, Inc.

Sources (1)

  • FDA UDI 2f348ee1-9231-44d8-bffb-e9193c3b52b1 33 fields · synced May 31, 2026