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

INSTA-BOND

K Number: K810517 · Decision Mar 24, 1981
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
191
Applicant Total
29
Review Days
27

Basic Information

Device Name
INSTA-BOND
K Number
K810517
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
LEE PHARMACEUTICALS
Date Received
February 25, 1981
Decision Date
March 24, 1981
Product Code
DYH
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
DYH Adhesive, Bracket And Tooth Conditioner, Resin

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Other Clearances by LEE PHARMACEUTICALS

K Number Device Name
K924378 RESTOBOND 4
K912256 PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT
K900809 LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS
K894315 RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT
K881903 PROSTHODENT VL
K873123 LEE COMPOSITE INLAY SYSTEM
K863157 RESTODENT POSTERIOR
K854882 PROTEC/VISIBLE LIGHT-CURED SEALANT/DENTAL RESTORAT
K844134 CLEANSE N BOND II
K844133 CLEANSE N BOND I
Search all 29 clearances from LEE PHARMACEUTICALS →