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Reicodent 02-5253

by devemed GmbH

Reicodent 02-5253 is a dental impression tray (FDA Class I; FDA product code EHY, Tray, Impression, Preformed) made by devemed GmbH, listed in FDA GUDID since 28 Apr 2020 (UDI-DI 04061644025534), 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 Number04061644025534 UDI-DI Date28 Apr 2020ListedStatusListed 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  • Withdrawn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
Reicodent
Generic name
Dental impression tray, reusable
Model / reference
02-5253
Description
Impression tray # 3 for toothed lower jaws perforated
Primary DI / UDI-DI
04061644025534
FDA product code
EHY
GMDN term
Dental impression tray, reusable
Device class
Class I
Regulation number
872.6880
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental impression tray, reusable

Similar devices

Other devices filed under FDA product code EHY (Tray, Impression, Preformed).

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)