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3D Dental PR135

by 3D Dental Designs and Development, LLC

3D Dental PR135 is a Class I device made by 3D Dental Designs and Development, LLC, listed in FDA GUDID since 27 Feb 2023 (UDI-DI 00817169029717), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817169029717 UDI-DI Date27 Feb 2023ListedStatusListed 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  • Withdrawn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
3D Dental
Generic name
Dental floss
Model / Ref / Catalog
PR135
Primary DI / UDI-DI
00817169029717
FDA product code
JES
GMDN term
Dental floss
Device class
Class I
Regulation number
872.6390
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from 3D Dental Designs and Development, LLC

See all devices from 3D Dental Designs and Development, LLC →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)