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Forefoot Solutions™

FDA UDI

Class I (US FDA UDI)

by Newdeal Sas

Identity

Trade Name
FOREFOOT SOLUTIONS™ FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
The depth gauge is used by the surgeon to choose the length of the screw or the staple to implant. FDA UDI
Model / Reference
997301ND FDA UDI
Description
The depth gauge is used by the surgeon to choose the length of the screw or the staple to implant. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780044888 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical depth gauge, reusable

Forefoot Solutions™ by Newdeal Sas — 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
Newdeal Sas

Sources (1)

  • FDA UDI e33bb578-23f9-4f22-bcec-3500769bbdb4 35 fields · synced Jun 1, 2026