FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Neowise

K Number: K260716 · Decision May 4, 2026
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
21
Review Days
60

Basic Information

Device Name
Neowise
K Number
K260716
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cefla S.C.
Date Received
March 5, 2026
Decision Date
May 4, 2026
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

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

View all

Other Clearances by Cefla S.C.

K Number Device Name
K252353 myray ProXIma X6
K230895 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,
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. →