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Gum®

FDA UDI

Class I (US FDA UDI)

by Sunstar Americas, Inc.

Identity

Trade Name
GUM® FDA UDI
Generic Name
Dental floss FDA UDI
Device Name
This standard US Ortho Kit for Professional Sales includes: * Code 632DB: Soft Pick US Professional 72 CT * Code 124PD: Orthodontic Toothbrush * Code 723PD: OrthoWax Unflavored 2 DZ * Code 1840PC Flossthreader * Code 1815PQB: Pro-Weave Mint, 4 yards * Code 3614PQ: Proxabrush Wide FDA UDI
Model / Reference
ORTHKITPRB FDA UDI
Description
This standard US Ortho Kit for Professional Sales includes: * Code 632DB: Soft Pick US Professional 72 CT * Code 124PD: Orthodontic Toothbrush * Code 723PD: OrthoWax Unflavored 2 DZ * Code 1840PC Flossthreader * Code 1815PQB: Pro-Weave Mint, 4 yards * Code 3614PQ: Proxabrush Wide FDA UDI

Identifiers

Primary DI / UDI-DI
00070942008143 FDA UDI
FDA Product Code
JES FDA UDI
EFW FDA UDI
EGD FDA UDI
JET FDA UDI
GMDN Term
Dental floss FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6390 FDA UDI
872.6855 FDA UDI
872.6890 FDA UDI
872.6650 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental flossBasic manual toothbrushPeriodontal pick/brush, reusableOrthodontic appliance relief material

Gum® by Sunstar Americas, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic appliance relief material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1457ee38-10b2-40cb-a1f7-8a15117e2481 34 fields · synced May 31, 2026