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Sterispine Lc

FDA UDI

Class II (US FDA UDI)

by Safe Orthopaedics

Identity

Trade Name
STERISPINE LC FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Model / Reference
KITLCC30-10 FDA UDI

Identifiers

Primary DI / UDI-DI
03760219912415 FDA UDI
510(k) Number
K133893 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metallic spinal interbody fusion cage

Sterispine Lc by Safe Orthopaedics — 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
Safe Orthopaedics

Sources (1)

  • FDA UDI 882e8846-83da-47d6-9c77-a82b65b23d8b 33 fields · synced Jun 1, 2026