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

FLEXITIME XTREME 2 HEAVY TRAY CARTRIDGE REFILL, FEXITIME XTREME 2 LIGHT TRAY CARTRIDGE REFILL

K Number: K101617 · Decision Sep 7, 2010
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
11
Review Days
90

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Basic Information

Device Name
FLEXITIME XTREME 2 HEAVY TRAY CARTRIDGE REFILL, FEXITIME XTREME 2 LIGHT TRAY CARTRIDGE REFILL
K Number
K101617
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, LLC
Date Received
June 9, 2010
Decision Date
September 7, 2010
Product Code
ELW
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
ELW Material, Impression

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Other Clearances by Heraeus Kulzer, LLC

K Number Device Name
K130647 XANTASIL DYNAMIX FAST SET CARTRIDGE -2 X 380ML; XANTASIL FAST SET CARTRIDGE -6 X 50ML
K123278 IBOND SELF ETCH BOTTLE ASSORTMENT, IBOND SELF ETCH BOTTLE VALUE PACK, IBOND SELF ETCH SINGLE DOSE ASSORTMENT, IBOND SELF
K120914 FLEXITIME FAST & SCAN LIGHT FLOW
K113574 FLEXITIME MONOPHASE PRO SCAN
K112501 VENUS PEARL PLT REFILL A1
K111832 PALADON ULTRA POWDER (PINK), PALADON ULTRA LIQUID
K110037 PALAXPRESS ULTRA POWDER (PINK); PALAXPRESS ULTRA LIQUID
K102770 FLEXTIME FAST & SCAN PUTTY, FLEXTIME FAST & SCAN LIGHT FLOW, FLEXTIME FAST & SCAN MEDIUM FLOW
K093575 GLUMA DESENSITIZER POWER GEL
K091635 VENUS DIAMOND FLOW
Search all 11 clearances from Heraeus Kulzer, LLC →