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

RESTODENT POSTERIOR

K Number: K863157 · Decision Sep 25, 1986
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
29
Review Days
41

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RESTODENT POSTERIOR
K Number
K863157
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Lee Pharmaceuticals
Date Received
August 15, 1986
Decision Date
September 25, 1986
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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

View all

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
K854882 PROTEC/VISIBLE LIGHT-CURED SEALANT/DENTAL RESTORAT
K844133 CLEANSE N BOND I
K844134 CLEANSE N BOND II
K843363 RESTODENT VL
Search all 29 clearances from Lee Pharmaceuticals →