FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇹 Italy

CEFLA Dental Micromotors: i-MMr, i-MMr L, i-MMr L FLUO, i-MMs, i-MMs FLUO; i-XR3, i-XR3 L, i-XR3 L FLUO, i-XS4,

K Number: K230895 · Decision Apr 1, 2024
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
60
Applicant Total
21
Review Days
367

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CEFLA Dental Micromotors: i-MMr, i-MMr L, i-MMr L FLUO, i-MMs, i-MMs FLUO; i-XR3, i-XR3 L, i-XR3 L FLUO, i-XS4,
K Number
K230895
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cefla S.C.
Date Received
March 31, 2023
Decision Date
April 1, 2024
Product Code
EBW
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
EBW Controller, Foot, Handpiece And Cord

Similar 510(k) Clearances

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

View all

Other Clearances by Cefla S.C.

K Number Device Name
K260716 Neowise
K252353 myray ProXIma X6
K231990 Apex Locator
K223794 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
K213022 CEFLA Dental Micromotors: i-MMr, i-MMr L, i-MMs, i-XR3, i-XR3 L, i-XS4, handy POWER, handy POWER LED, implantor LED
K220664 NewTom 7G
K214084 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
K200688 hyperion X5, NewTom GO, X-RADiUS COMPACT
K190496 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
K183448 NewTom 5G XL
Search all 21 clearances from Cefla S.C. →