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Monkey Rings™ External Fixation System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
Monkey Rings™ External Fixation System FDA UDI
Generic Name
Orthopaedic fixation implant alignment tool FDA UDI
Device Name
ARTICULATING WRENCH FDA UDI
Model / Reference
P45-514-0001 FDA UDI
Description
ARTICULATING WRENCH FDA UDI

Identifiers

Catalog Number
P45-514-0001 FDA UDI
Primary DI / UDI-DI
00889795116475 FDA UDI
510(k) Number
K212895 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic fixation implant alignment tool FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic fixation implant alignment tool

Monkey Rings™ External Fixation System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation implant alignment tool.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 05bb3812-e336-45f3-b4a2-8385b61d13c1 35 fields · synced Jun 6, 2026