FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TENAX WHITE POST

K Number: K993545 · Decision Apr 14, 2000
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
34
Applicant Total
21
Review Days
178

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Basic Information

Device Name
TENAX WHITE POST
K Number
K993545
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3810
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Coltene/Whaledent, Inc.
Date Received
October 19, 1999
Decision Date
April 14, 2000
Product Code
ELR
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
ELR Post, Root Canal

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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
K000311 PARAPOST FIBER WHITE
K993710 MODIFICATION OF PARAPOST CEMENT
K993835 PARAPOST SYSTEM STERILIZABLE ORGANIZER
Search all 21 clearances from Coltene/Whaledent, Inc. →