← Back to catalogue

23mm x 10mm x 10mm PLIF with Inserter

FDA UDI

Class II (US FDA UDI)

by Xenco Medical Llc

Identity

Trade Name
23mm x 10mm x 10mm PLIF with Inserter FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
23mm x 10mm x 10mm PLIF with Inserter FDA UDI
Model / Reference
XM-011-2310 FDA UDI
Description
23mm x 10mm x 10mm PLIF with Inserter FDA UDI

Identifiers

Primary DI / UDI-DI
B064XM01123101 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable 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

Yes

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

Yes

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

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

23mm x 10mm x 10mm PLIF with Inserter by Xenco Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

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
Xenco Medical Llc

Sources (1)

  • FDA UDI 3c6a1afc-5c9d-4a0a-aa3f-bda542167cb8 34 fields · synced May 31, 2026