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Gum® 875

by Sunstar Americas, Inc.

Gum® 875 (SM) is a Class I device made by Sunstar Americas, Inc., listed in FDA GUDID since 28 Jul 2026 (UDI-DI 00070942008334), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00070942008334 UDI-DI Date28 Jul 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Gum®
Generic name
Dental floss
Model / Ref / Catalog
875, SM
Primary DI / UDI-DI
00070942008334
FDA product code
JES
GMDN term
Dental floss
Device class
Class I
Regulation number
872.6390
GUDID distribution status
In Commercial Distribution
Size
Height — 70.81 Millimeter

Similar devices

Other devices filed under FDA product code JES (FLOSS, DENTAL).

Other devices from Sunstar Americas, Inc.

See all devices from Sunstar Americas, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)