JuggerKnot Soft Anchors

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name: JuggerKnot Soft Anchors FDA UDI
Generic Name: Suturing unit, single-use FDA UDI
Model / Reference: 912029 FDA UDI

Identifiers

Catalog Number: 912029 FDA UDI
Primary DI / UDI-DI: 00880304522350 FDA UDI
FDA Product Code: JDR FDA UDI
MBI FDA UDI
GMDN Term: Suturing unit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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 Safe FDA UDI

Category: Suturing unit, single-use

JuggerKnot Soft Anchors by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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OverStitch NXT Endoscopic Suturing System — Apollo Endosurgery · Class II
SlingShot — Stryker Corp. · Class I
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JUGGERKNOT SOFT ANCHORS — Biomet Sports Medicine · 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: Biomet Orthopedics, Inc.

Sources (1)

FDA UDI 2eee4c50-0be0-4e10-8d04-c525b049729b 35 fields · synced Jun 8, 2026