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TenoTac Soft Tissue Fixation System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
TenoTac Soft Tissue Fixation System FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
TenoTac Single Use Male Implant Inserter T15 Driver, 40mm Inserter Wire FDA UDI
Model / Reference
P42-931-T154 FDA UDI
Description
TenoTac Single Use Male Implant Inserter T15 Driver, 40mm Inserter Wire FDA UDI

Identifiers

Catalog Number
P42-931-T154 FDA UDI
Primary DI / UDI-DI
00889795057211 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

TenoTac Soft Tissue Fixation System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 1074b066-9f00-4c61-9404-4a36e5f8463b 34 fields · synced May 30, 2026