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Maxcem Elite Chroma 36300

by Kerr Corporation

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 Number10841396102186 UDI-DI Date26 May 2020ListedStatusListed 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  • Withdrawn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
Maxcem Elite Chroma
Generic Name
Dental composite resin
Model / Reference
36300
Primary DI / UDI-DI
10841396102186
FDA Product Code
EMA
GMDN Term
Dental composite resin
Device Class
Class II
Regulation Number
872.3275
GUDID distribution status
In Commercial Distribution
Size
Weight — 10 Gram

Related devices

Category: Dental composite resin

Other devices from Kerr Corporation

See all devices from Kerr Corporation →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No