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Sunshine Diamonds G308L

by Dr. Hopf GmbH & Co. KG

Sunshine Diamonds G308L is a Class I device made by Dr. Hopf GmbH & Co. KG, listed in FDA GUDID since 30 Jun 2023 (UDI-DI ESUNG308L8), 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 NumberESUNG308L8 UDI-DI Date30 Jun 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sunshine Diamonds
Generic name
Dental abrasive strip, single-use
Model / reference
G308L
Primary DI / UDI-DI
ESUNG308L8
FDA product code
EHM
GMDN term
Dental abrasive strip, single-use
Device class
Class I
Regulation number
872.6010
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive strip, single-use

Other devices from Dr. Hopf GmbH & Co. KG

See all devices from Dr. Hopf GmbH & Co. KG →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)