LOSPA IS Spinal System

FDA UDI

Class I (US FDA UDI)

by Corentec Co., Ltd

Identity

Trade Name: LOSPA IS Spinal System FDA UDI
Generic Name: Orthopaedic graft inserter, reusable FDA UDI
Device Name: PLIF FINAL IMPACTOR FDA UDI
Model / Reference: SI.C50.0020 FDA UDI
Description: PLIF FINAL IMPACTOR FDA UDI

Identifiers

Primary DI / UDI-DI: 08800017275406 FDA UDI
FDA Product Code: HWA FDA UDI
GMDN Term: Orthopaedic graft inserter, reusable 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: Orthopaedic graft inserter, reusable

LOSPA IS Spinal System by Corentec Co., Ltd — 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: Corentec Co., Ltd

Sources (1)

FDA UDI 067294c0-7556-493c-950d-ed9c01b1b7c6 34 fields · synced May 30, 2026