Re+Line Bunion Correction System

FDA UDI

Class II (US FDA UDI)

by Medartis Inc.

Identity

Trade Name: Re+Line Bunion Correction System FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name: 25mm X 8 Re+Line Kit FDA UDI
Model / Reference: RS-25815K FDA UDI
Description: 25mm X 8 Re+Line Kit FDA UDI

Identifiers

Primary DI / UDI-DI: 00817701020073 FDA UDI
FDA Product Code: HRS FDA UDI
HWC FDA UDI
JDR FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Re+Line Bunion Correction System by Medartis Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Medartis Inc.

Sources (1)

FDA UDI 7f6deb7d-b07e-4940-b658-ea9420e59581 33 fields · synced Jun 6, 2026