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Lucent

FDA UDI

Class II (US FDA UDI)

by Spinal Elements, Inc.

Identity

Trade Name
LUCENT FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
8MM X 22MM X 8MM 5° CAGE FDA UDI
Model / Reference
11822-508 FDA UDI
Description
8MM X 22MM X 8MM 5° CAGE FDA UDI

Identifiers

Primary DI / UDI-DI
00840606113243 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Polymeric spinal interbody fusion cage

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

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9ab2ebff-d376-482c-901d-93fd658df1a1 34 fields · synced Jun 6, 2026