Ø7.5mm x 50mm Pedicle Micro Reduction Screw with Set Screw Package

FDA UDI

Class II (US FDA UDI)

by Xenco Medical Llc

Identity

Trade Name: Ø7.5mm x 50mm Pedicle Micro Reduction Screw with Set Screw Package FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: Ø7.5mm x 50mm Cannulated Micro Extended Pedicle Screw with Set Screw Package FDA UDI
Model / Reference: XM-225-7550 FDA UDI
Description: Ø7.5mm x 50mm Cannulated Micro Extended Pedicle Screw with Set Screw Package FDA UDI

Identifiers

Primary DI / UDI-DI: B064XM22575501 FDA UDI
FDA Product Code: NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
KWQ FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3060 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable Spinal bone set screw

Ø7.5mm x 50mm Pedicle Micro Reduction Screw with Set Screw Package by Xenco Medical Llc — Class II — FDA UDI — listed in FDA GUDID

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Xenco Medical Llc

Sources (1)

FDA UDI 8f64ff48-b030-4fa6-aa79-370558228622 34 fields · synced May 30, 2026