ProAM ALIF System

FDA UDI

Class I (US FDA UDI)

by Pro Surgical, Inc.

Identity

Trade Name: ProAM ALIF System FDA UDI
Generic Name: Spinal implant trial FDA UDI
Device Name: ALIF Trial - 38mm x 27mm x 20mm, 6° FDA UDI
Model / Reference: LN-013827-0620 FDA UDI
Description: ALIF Trial - 38mm x 27mm x 20mm, 6° FDA UDI

Identifiers

Catalog Number: LN-013827-0620 FDA UDI
Primary DI / UDI-DI: 00810152902141 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Spinal implant trial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal implant trial

ProAM ALIF System by Pro Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Pro Surgical, Inc.

Sources (1)

FDA UDI 5c904d28-eabe-496d-a602-f57135e0043e 34 fields · synced Jun 8, 2026