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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
Bone holding forceps FDA UDI
Device Name
The Scarf clamp is used in Scarf osteotomy, where its specific design (asymmetrical jaws) allows variable lateral displacement and bone fragments holding in the correct position prior to screw fixation. FDA UDI
Model / Reference
119105ND FDA UDI
Description
The Scarf clamp is used in Scarf osteotomy, where its specific design (asymmetrical jaws) allows variable lateral displacement and bone fragments holding in the correct position prior to screw fixation. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780051862 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Bone holding forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Bone holding forceps

Forefoot Solutions™ by Newdeal Sas — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Newdeal Sas

Sources (1)

  • FDA UDI 192d8677-939e-42c1-b142-2ab54cc59c0b 35 fields · synced Jun 8, 2026