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

PONTIC PAINT

K Number: K130237 · Decision Apr 5, 2013
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
143
Applicant Total
32
Review Days
64

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Basic Information

Device Name
PONTIC PAINT
K Number
K130237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Reliance Orthodontic Products, Inc.
Date Received
January 31, 2013
Decision Date
April 5, 2013
Product Code
NXC
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
NXC Aligner, Sequential

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K123348 CLEAR ALIGNER ADHESIVE
K111814 PADLOCK
K101951 LIGHT CURE RETAINER
K083051 FLOWTAIN & FLOWTAIN LV
K073243 LED PRO SEAL
K071688 RELIANCE S.E.P.
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