Charisma

FDA 510(k) K910263 · Kulzer, Inc.

Substantially Equivalent

510(k) numberK910263

Submission

Device name
Charisma
Applicant
Kulzer, Inc.
Irvine, CA, US
Received
January 22, 1991
Decision date
June 3, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EBF – Material, Tooth Shade, Resin
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3690
Specialty
Dental

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K260805Dual CoreEBF · Traditional Vericom Co., Ltd.05/11/2026SE
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K230644Signum opaque FEBF · Traditional 09/07/2023SE
K220605Venus Bulk Flow ONEEBF · Special 04/21/2022SE
K905058Palavit LEBH · Traditional 06/06/1991SE
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Questions and answers

When was Charisma cleared by the FDA?

Charisma (K910263) received a 510(k) decision of Substantially Equivalent on June 3, 1991, 132 days after the submission was received.

What is the product code of K910263?

The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.