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Renamel Microhybrid Basic Kit 606005

by Cosmedent, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD7796060053 UDI-DI Date22 Sep 2016ListedStatusListed 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  • Withdrawn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
Renamel Microhybrid Basic Kit
Generic Name
Dental composite resin
Model / Ref / Catalog
606005
Primary DI / UDI-DI
D7796060053
GMDN Term
Dental composite resin
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: Renamel Microhybrid Composite

Other devices from Cosmedent, Inc.

See all devices from Cosmedent, Inc. →

Properties

  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No