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Morelli 35.11.001

by Dental Morelli Ltda

Morelli 35.11.001 is a Class I device made by Dental Morelli Ltda, listed in FDA GUDID since 15 May 2021 (UDI-DI 07895742000851), registry data as of 13 Nov 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 13 Nov 2026.

Regulatory status

as of registry sync 13 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07895742000851 UDI-DI Date15 May 2021ListedStatusListed 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  • Withdrawn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
Morelli
Generic name
Orthodontic clasp, metal, custom-made
Model / Ref / Catalog
35.11.001
Primary DI / UDI-DI
07895742000851
FDA product code
EHO
GMDN term
Orthodontic clasp, metal, custom-made
Device class
Class I
Regulation number
872.3165
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Orthodontic clasp, metal, custom-made

Similar devices

Other devices filed under FDA product code EHO (BAR, PREFORMED).

Other devices from Dental Morelli Ltda

See all devices from Dental Morelli Ltda →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)