Hnm Medical

FDA UDI

Class II (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name: HNM MEDICAL FDA UDI
Generic Name: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name: ETHOS MEDIAL ANCHOR, PEEK, 6.5mm x 15mm, (2) #2 SUTURE, W/MO-6 NEEDLES FDA UDI
Model / Reference: HNM-33-151697 FDA UDI
Description: ETHOS MEDIAL ANCHOR, PEEK, 6.5mm x 15mm, (2) #2 SUTURE, W/MO-6 NEEDLES FDA UDI

Identifiers

Catalog Number: HNM-33-151697 FDA UDI
Primary DI / UDI-DI: 00842962105191 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

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Hnm Medical by Hnm Stainless, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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JuggerKnot Soft Anchors — Biomet Orthopedics, Inc. · Class II

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: Hnm Stainless, Llc.

Sources (1)

FDA UDI ce232bf6-b628-467c-afb8-c5a47bb9cfb8 34 fields · synced Jun 6, 2026