SimpliShade 37007

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841396198953 UDI-DI	Date24 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: SimpliShade
Generic name: Dental composite resin
Model / reference: 37007

Primary DI / UDI-DI: 00841396198953
FDA product code: EBF
GMDN term: Dental composite resin

Device class: Class II
Regulation number: 872.3690
GUDID distribution status: In Commercial Distribution

Size: Weight — 5 Gram

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Properties

Single use
Prescription use
Lot / batch number
Expiration date

Other properties (11)

Supplied sterile: No
Sterilise before use: 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
Manufacturing date: No