FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE

K Number: K934265 · Decision Jan 21, 1994
Classifications
1
FEI Numbers
168
Registration Numbers
168
Same Product Code
29
Applicant Total
20
Review Days
143

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Basic Information

Device Name
FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE
K Number
K934265
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Flexmedics
Date Received
August 31, 1993
Decision Date
January 21, 1994
Product Code
DZC
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
DZC Wire, Orthodontic

Similar 510(k) Clearances

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

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Other Clearances by Flexmedics

K Number Device Name
K990765 FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO
K964955 FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKING
K952430 FINESSE GUIDEWIRE CORONARY
K943390 FLEXFINDER GUIDEWIRE
K942074 FLEXFINDER GUIDEWIRE
K912843 FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBE
K910674 FLEXMEDICS MALLEABLE CANNULA
K895899 FLEXMEDICS GUIDEWIRE .012 ONLY
K893626 FLEXMEDICS GUIDEWIRE
K885086 TIN COATED NITI ORTHODONTIC ARCH WIRES
Search all 20 clearances from Flexmedics →