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

EVERSTICK ORTHO

K Number: K021126 · Decision May 13, 2002
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
9
Review Days
35

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Basic Information

Device Name
EVERSTICK ORTHO
K Number
K021126
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stick Tech , Ltd.
Date Received
April 8, 2002
Decision Date
May 13, 2002
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

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

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Other Clearances by Stick Tech , Ltd.

K Number Device Name
K051953 EVERSTICK A&O
K031341 STICK FLOW
K030820 EVERSTICK POST
K030072 EVERSTICK PERIO
K011788 EVERSTICK
K011799 EVERSTICKNET
K003334 STICK NET
K003333 STICK