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OC JuggerKnot Soft Anchor

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name
OC JuggerKnot Soft Anchor FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
Soft Anchor FDA UDI
Model / Reference
110048376 FDA UDI
Description
Soft Anchor FDA UDI

Identifiers

Primary DI / UDI-DI
00840277402905 FDA UDI
FDA Product Code
MBI FDA UDI
MAI 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
888.3030 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

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

OC JuggerKnot Soft Anchor by Riverpoint Medical Llc — Class II — 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

Sources (1)

  • FDA UDI 16a0141b-3da5-440a-9539-a68bd629bfce 33 fields · synced Jun 1, 2026