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

COLTENE A.R.T. BOND

K Number: K922615 · Decision Aug 3, 1992
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
21
Review Days
62

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Basic Information

Device Name
COLTENE A.R.T. BOND
K Number
K922615
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Coltene/Whaledent, Inc.
Date Received
June 2, 1992
Decision Date
August 3, 1992
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KLE), ordered by most recent decision date.

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Other Clearances by Coltene/Whaledent, Inc.

K Number Device Name
K071632 PERFECT TISSUE CONTOURING SYSTEM II
K051660 DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM
K040551 COLTOLUX LED CURING LIGHT
K033760 ONE COAT SE BOND
K031752 COLTOSOL F
K013400 SYNERGY FLOW
K003034 COLTENE AURA COMPOMER RESTORATIVE SYSTEM
K993545 TENAX WHITE POST
K000311 PARAPOST FIBER WHITE
K993710 MODIFICATION OF PARAPOST CEMENT
Search all 21 clearances from Coltene/Whaledent, Inc. →