Atlas FDA

PROV-KB

FDA 510(k) clearance K960938 · decided 1996-04-18

Clearance details

K-number
K960938
Device name
PROV-KB
Applicant
Silicon-Und Composite Spezialitaten GmbH
Decision
Substantially Equivalent
Date received
1996-03-08
Decision date
1996-04-18
Days to decision
41 days
Clearance type
Traditional
Product code
EBG
Device class
2
Regulation number
872.3770
Medical specialty
Dental
Advisory committee
Dental
Location
Bokholt-Hanredder, DE
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Dura-Arch (K261261)Hangzhou SHINING3D Dental Technology Co., Ltd.2026-04-17
“FLNT Base” and “FLNT Temp” (K253380)Liaoning Upcera Co., Ltd.2026-03-02
TempFIT Temporary Crown and Bridge Resin (K251271)Rizhao Huge Biomaterials Company, Ltd.2025-06-23
DentaTOOTH (K243370)Asiga Pty, Ltd.2025-05-05
Evoblock, Perléon (K243621)Evoden Indústria Comércio Importação E Exportação2025-04-22
TEMP MASTER, PMMA-based dental resin (K243951)Taiwan Dental Materials Co., Ltd.2025-02-21
PrimmaArt (K231859)Dentscare Ltda2024-11-26
Digital Temp (K242559)Sprintray, Inc.2024-11-26
Premium Teeth Resin (K240538)Formlabs Ohio, Inc.2024-07-19
Fixtemp® C&B 4:1 (K241226)Dreve Denatmid GmbH2024-05-31
dima Print Teeth & Temp (K233868)Kulzer, LLC2024-05-23
PMMA BLOCK (K223706)Huliang(Shanghai) Bio-Tech Co., Ltd.2023-05-12

Recalls involving this device

No recalls on record reference this clearance.