Monster Screw System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name: Monster Screw System FDA UDI
Generic Name: Implantable bone washer FDA UDI
Device Name: 3.0 Flat Washer, Mini Monster FDA UDI
Model / Reference: P20-030-DW00 FDA UDI
Description: 3.0 Flat Washer, Mini Monster FDA UDI

Identifiers

Catalog Number: P20-030-DW00 FDA UDI
Primary DI / UDI-DI: 00889795001153 FDA UDI
FDA Product Code: HTN FDA UDI
GMDN Term: Implantable bone washer 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

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Implantable bone washer

Monster Screw System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable bone washer.

ISOLA — Depuy Spine, Inc. · Class II
Spiked Gridlock Screw Washer — Trilliant Surgical LLC · Class II
ALPHALOK Plating System — Vilex, Inc. · Class II
FLAT WASHER — Biomet Orthopedics, Inc. · Class II
Fixcet Spinal Facet Screw System — Xtant Medical Holdings, Inc. · U
LEOS Cannulated Screw System — Tyber Medical · Class II
FacetLink System — WALDEMAR LINK GmbH & Co. KG · U
Washers — Trimed, 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: Paragon 28

Sources (1)

FDA UDI c9d45d20-43c8-4d33-b9fe-14f04eafbc5a 35 fields · synced Jun 1, 2026