← Back to catalogue

LOSPA IS Spinal System

FDA UDI

Class II (US FDA UDI)

by Corentec Co., Ltd

Identity

Trade Name
LOSPA IS Spinal System FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
LOSPA IS DLIF Cage (Non-sterile) FDA UDI
Model / Reference
SC.V01.6016 FDA UDI
Description
LOSPA IS DLIF Cage (Non-sterile) FDA UDI

Identifiers

Primary DI / UDI-DI
08800017221755 FDA UDI
510(k) Number
K170243 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Polymeric 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

LOSPA IS Spinal System by Corentec Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Corentec Co., Ltd

Sources (1)

  • FDA UDI 02662916-c3ea-422b-bc59-0206a7f469b0 35 fields · synced Jun 8, 2026