Iconix

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name: Iconix FDA UDI
Generic Name: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name: Iconix HA+ 2 TT, 2.3mm Anchor with 2 Strands 1.8mm XBraid TT (Black/White, White/Black) FDA UDI
Model / Reference: 3911-523-730HA FDA UDI
Description: Iconix HA+ 2 TT, 2.3mm Anchor with 2 Strands 1.8mm XBraid TT (Black/White, White/Black) FDA UDI

Identifiers

Primary DI / UDI-DI: 00812444029741 FDA UDI
FDA Product Code: MBI FDA UDI
GMDN Term: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 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

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

MRI Safety

MR Safe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Iconix by Riverpoint Medical Llc — 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: Riverpoint Medical Llc

Sources (1)

FDA UDI 14e25bf0-8a92-4a8b-92bb-e4e55d1262e7 33 fields · synced May 31, 2026