ProLift Lateral

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name: ProLift Lateral FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Model / Reference: 151-1092 FDA UDI

Identifiers

Primary DI / UDI-DI: 00190837105198 FDA UDI
510(k) Number: K193258 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Metallic 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

FDA UDI

Single Use

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Metallic spinal interbody fusion cage

The ProLift Lateral is a highly advanced, implantable metallic spinal interbody fusion cage designed to provide optimal bone fusion and osseointegration in patients with degenerative disc disease. This device features a hollow, porous design that allows for therapeutic spinal bone fusion, typically in conjunction with bone grafting. The cage is made of titanium (Ti) and provides mechanical stability, making it an ideal solution for intervertebral disc removal procedures.

Similar devices

Also classified as Metallic spinal interbody fusion cage.

KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
CoRoent — Nuvasive, Inc. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
MectaLIF 3D — Medacta International · Class II
PILLAR TL — Orthofix US LLC · Class II
Solar™ Interbody Fusion System — Degen Medical · Class II
Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II

Cleared under the same submission

K193258 also covers:

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: Life Spine, Inc.

Sources (1)

FDA UDI ccf415b6-331d-484f-b6ab-5aa42938d3c4 33 fields · synced Jul 21, 2026