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

REPLICA DENTAL COMPOSIT

K Number: K771880 · Decision Oct 20, 1977
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
11
Review Days
16

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Basic Information

Device Name
REPLICA DENTAL COMPOSIT
K Number
K771880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Hoyt Laboratories
Date Received
October 4, 1977
Decision Date
October 20, 1977
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

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Other Clearances by Hoyt Laboratories

K Number Device Name
K820738 LUSTRALLOY
K811154 HOYT ECONO-TRAY
K810830 HOYT COTTON ROLLS
K780834 PREVI DENT PROPHYLAXIS MINT NDC
K771881 REPLICA BONDING AGENT
K771883 REPLICA ACID-ETCH
K771882 REPLICA DENTAL COMPOSITE-RADIOPAQUE
K771185 PERIODONTIC TOOTHBRUSH, #0126-0190-00
K771184 TOOTHBRUSH, ORTHODONTIC, #0126-0189-00
K771183 TOOTHBRUSH, PEDODONTIC, #0126-0188-00
Search all 11 clearances from Hoyt Laboratories →