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

HELIOSIT-ORTHODONTIC

K Number: K823409 · Decision Jan 21, 1983
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
17
Review Days
67

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Basic Information

Device Name
HELIOSIT-ORTHODONTIC
K Number
K823409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Vivadent (Usa), Inc.
Date Received
November 15, 1982
Decision Date
January 21, 1983
Product Code
DYH
Advisory Committee
Dental
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
DYH Adhesive, Bracket And Tooth Conditioner, Resin

Similar 510(k) Clearances

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Other Clearances by Vivadent (Usa), Inc.

K Number Device Name
K863831 VIVADENT FILPIN
K813015 HELIOSEAL
K802679 SILANIT
K802682 CONTACT SEAL
K802681 HELIOBOND
K802683 HELIOSIT
K802684 HELIOMAT
K802685 REOLIT
K802680 ISOPAST-DS
K801227 SILICAP
Search all 17 clearances from Vivadent (Usa), Inc. →