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

KELES FACEMASK

K Number: K041718 · Decision Oct 15, 2004
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
35
Applicant Total
13
Review Days
113

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Basic Information

Device Name
KELES FACEMASK
K Number
K041718
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5500
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Great Lakes Orthodontics, Ltd.
Date Received
June 24, 2004
Decision Date
October 15, 2004
Product Code
DZB
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
DZB Headgear, Extraoral, Orthodontic

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Other Clearances by Great Lakes Orthodontics, Ltd.

K Number Device Name
K172765 Smart Moves Complete
K150702 Exceed Tx
K083479 BIOCRYL X
K040881 METACRYL
K033632 VARIFLEX
K922818 SNORE-NO-MORE
K925275 SOFT DENTURE RELINE MATERIAL ELASTOLINE
K870908 STEADY RESIN
K861424 ADAPTABLE CLASS III MASK
K840805 ORAL SAFE
Search all 13 clearances from Great Lakes Orthodontics, Ltd. →