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Lesser Metatarsal Shortening System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Lesser Metatarsal Shortening System FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
Met Shortening Depth Gage FDA UDI
Model / Reference
P35-980-1000 FDA UDI
Description
Met Shortening Depth Gage FDA UDI

Identifiers

Catalog Number
P35-980-1000 FDA UDI
Primary DI / UDI-DI
00889795124166 FDA UDI
FDA Product Code
HTJ FDA UDI
GMDN Term
Surgical depth gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4300 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical depth gauge, reusable

Lesser Metatarsal Shortening System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical depth gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 4134e9fe-7c38-480d-b852-363a9b20cde8 34 fields · synced Jun 1, 2026