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Linx

FDA UDI

Class III (US FDA UDI)

by Torax Medical, Inc.

Identity

Trade Name
LINX FDA UDI
Generic Name
Gastro-oesophageal antireflux prosthesis FDA UDI
Device Name
LINX Reflux Management System FDA UDI
Model / Reference
LXMC15 FDA UDI
Description
LINX Reflux Management System FDA UDI

Identifiers

Catalog Number
LXMC15 FDA UDI
Primary DI / UDI-DI
00855106005356 FDA UDI
PMA Number
P100049 FDA UDI
FDA Product Code
LEI FDA UDI
GMDN Term
Gastro-oesophageal antireflux prosthesis FDA UDI

Classification

Device Class
Class III 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Gastro-oesophageal antireflux prosthesis

Linx by Torax Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-oesophageal antireflux prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Torax Medical, Inc.

Sources (1)

  • FDA UDI 08015bc1-87c2-4bbf-8742-5dbb99896fe5 37 fields · synced Jun 8, 2026