HEALIX ADVANCE PEEK ANCHOR w/PERMATAPE PERMACORD

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name: HEALIX ADVANCE PEEK ANCHOR w/PERMATAPE PERMACORD FDA UDI
Generic Name: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name: PEEK Anchor with (1) 2.5mm Blue PERMATAPE Braided Flat Suture, 38 inches (96 cm) and (1) White/Black, Size 2 (5 metric) PERMACORD Braided Suture, 36 inches (91cm), (1) Utility Shuttle Suture FDA UDI
Model / Reference: 222363 FDA UDI
Description: PEEK Anchor with (1) 2.5mm Blue PERMATAPE Braided Flat Suture, 38 inches (96 cm) and (1) White/Black, Size 2 (5 metric) PERMACORD Braided Suture, 36 inches (91cm), (1) Utility Shuttle Suture FDA UDI

Identifiers

Catalog Number: 222363 FDA UDI
Primary DI / UDI-DI: 10886705027835 FDA UDI
510(k) Number: K170639 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

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

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

HEALIX ADVANCE PEEK ANCHOR w/PERMATAPE PERMACORD by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Hi-Fi — Conmed Corporation · Class II
FLIPTIGHT LOOP — RIVERPOINT MEDICAL LLC · Class II
Ecobone — Bonegraft Biomaterials Co. · Class III
fX — Bonegraft Biomaterials Co. · Class III
GII PANACRYL — DePuy Mitek, Inc. · Class II
Power Button Adjustable Loop — RIVERPOINT MEDICAL LLC · Class II
SignaLoc Screw — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
JuggerKnot Soft Anchors — Biomet Orthopedics, Inc. · Class II

Cleared under the same submission

K170639 also covers:

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: Medos International Sàrl

Sources (1)

FDA UDI 528c23e2-c6f7-428d-bcf2-f24aa026da29 36 fields · synced May 30, 2026