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PLIF Cage

FDA UDI

Class II (US FDA UDI)

by Eisertech, LLC

Identity

Trade Name
PLIF Cage FDA UDI
Generic Name
Metallic spinal fusion cage, non-sterile FDA UDI
Device Name
Non-Lordotic TPLIF Cage, Titanium 25AP X 09ML X 12HT FDA UDI
Model / Reference
100149-250912 FDA UDI
Description
Non-Lordotic TPLIF Cage, Titanium 25AP X 09ML X 12HT FDA UDI

Identifiers

Catalog Number
100149-250912 FDA UDI
Primary DI / UDI-DI
B523100149250912 FDA UDI
510(k) Number
K113478 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Metallic spinal fusion cage, non-sterile 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Metallic spinal fusion cage, non-sterile

PLIF Cage by Eisertech, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal fusion cage, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eisertech, LLC

Sources (1)

  • FDA UDI 1e6cab30-d8cf-4e37-875e-975476c66ad3 35 fields · synced May 31, 2026