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OneLIF™

FDA UDI

Class II (US FDA UDI)

by Novapproach Spine

Identity

Trade Name
OneLIF™ FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
OneLIF Interbody, Medium, 19 Degree, 16mm X 8mm FDA UDI
Model / Reference
010-219-1608 FDA UDI
Description
OneLIF Interbody, Medium, 19 Degree, 16mm X 8mm FDA UDI

Identifiers

Catalog Number
010-219-1608 FDA UDI
Primary DI / UDI-DI
G07001021916080 FDA UDI
510(k) Number
K211769 FDA UDI
FDA Product Code
OVD FDA UDI
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

No

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

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

Category: Metallic spinal interbody fusion cage

OneLIF™ by Novapproach Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novapproach Spine

Sources (1)

  • FDA UDI e5a4fee6-9468-4f56-a2ce-f75cc1f860c7 36 fields · synced Jun 8, 2026