FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DENTIN BONDING SYSTEM

K Number: K894994 · Decision Oct 24, 1989
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
28
Review Days
77

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Basic Information

Device Name
DENTIN BONDING SYSTEM
K Number
K894994
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Cosmedent, Inc.
Date Received
August 8, 1989
Decision Date
October 24, 1989
Product Code
KLE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KLE Agent, Tooth Bonding, Resin

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Other Clearances by Cosmedent, Inc.

K Number Device Name
K240714 Insure® Universal; Insure® Universal Automix
K222435 Renamel® Microhybrid ;Renamel® Flowable Microhybrid
K211259 Renamel Bulkfill
K172707 Renamel Microfill
K163480 Renamel NANO +plus
K092730 COSMEDENT BRUSHABLE COMPOSITE
K070583 NANO COMPOSITE
K060881 TEMPORARY CROWN & BRIDGE RESIN
K052263 MULTIPLE (TOOTH DESENSITIZER)
K052501 MULTIPLE RESIN TOOTH BONDING AGENT
Search all 28 clearances from Cosmedent, Inc. →