SilTrax AS Retraction Cord 10/2

FDA UDI

Class U (US FDA UDI)

by Pascal Company, Inc.

Identity

Trade Name: SilTrax AS Retraction Cord 10/2 FDA UDI
Generic Name: Gingival retraction cord, non-medicated FDA UDI
Device Name: Braided Gingival Retraction Cord with Aluminum Sulfate, 72 inches, Size: 10/2 FDA UDI
Model / Reference: 07120 FDA UDI
Description: Braided Gingival Retraction Cord with Aluminum Sulfate, 72 inches, Size: 10/2 FDA UDI

Identifiers

Catalog Number: 07120 FDA UDI
Primary DI / UDI-DI: 00310866000350 FDA UDI
FDA Product Code: MVL FDA UDI
GMDN Term: Gingival retraction cord, non-medicated FDA UDI

Classification

Device Class: U FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Gingival retraction cord, non-medicated

SilTrax AS Retraction Cord 10/2 by Pascal Company, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Smartcord 2 — EASTDENT Co., Ltd · Class I
roeko Retracto / braided / non-impregnated, x-fine (0), 225 cm — Coltène/Whaledent GmbH + Co. KG · Class I
Hilo de retracción tejido Nº2 Dentaflux — J RIPOLL SL · Class I
Hilo de retracción tejido Nº00 Dentaflux — J RIPOLL SL · Class I
Henry Schein — HENRY SCHEIN, INC. · U
roeko Stay-put / non-impregnated, x-fine (0), 183 cm — Coltène/Whaledent GmbH + Co. KG · Class I
G-DENT Retraction Cord N.000 — UAB "Medicinos linija" · Class I
Mouth Prop — Huanghua Promisee Dental Co.Ltd. · Class I

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 U	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Pascal Company, Inc.

Sources (1)

FDA UDI 25b21fe8-844f-4cad-bf8c-9b2f5816db85 36 fields · synced May 30, 2026