FDA.reportPublic FDA data

CFlex™

Primary DI
00840432200018
Brand
CFlex™
Company
Verathon Medical (Canada) ULC
Model
Single-Use Cystoscope, Reverse Deflection
Catalog number
0570-0459
Device description
CFlex™ Single-Use Cystoscope, Reverse Deflection
Published
2026-05-15
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FAJCystoscope And Accessories, Flexible/Rigid

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FAJCystoscope And Accessories, Flexible/RigidGastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K253696000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K253696000CFlex Cystoscope - Standard Deflection (0570-0455); CFlex Cystoscope - Reverse Deflection (0570-0456); CystoView Monitor (0570-0465)Verathon Medical (Canada) Ulc2026-05-11FAJ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10840432200015PackageGS15In Commercial Distribution
00840432200018PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1084043220001510840432200015
00840432200018008404322000188404322000180840432200018

GMDN Terms#

Term, Definition table
TermDefinition
Flexible video cystoscope, single-useA sterile endoscope with a flexible inserted portion intended for the visual examination and treatment of the bladder and the urinary tract by introduction through the urethra. Anatomical images are transmitted from a distal camera and displayed on a monitor. It is typically used to examine/diagnose incontinence, urinary retention, recurrent urinary tract infections, and/or to remove tissue specimens/stones/small tumours from the bladder; it may have specialized tools for functions such as ureteral stent removal. This is a single-use device.

Regulatory Flags#

DUNS number
243738320
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00879123006561GlideScope®Video Baton 2.0 Large (3-4)0570-03822022-12-08
00879123007797GlideScope®Video Baton QC Large0570-04172022-12-08
00879123009012BFlex™BFlex™ 2 SamplePro™0574-02632026-05-29
00879123009340GlideScope®GlideScope® Core™ 10 FHD Essential Configuration0270-1212-FHD2026-05-29
00879123009357GlideScope®GlideScope® Core™ 15 FHD Essential Configuration0270-1213-FHD2026-05-29
00840432200056Verathon®Verathon® Essential Workstation0800-07002026-05-28
00840432200001CFlex™Single-Use Cystoscope, Standard Deflection0570-04552026-05-15
00840432200063CystoView™Essential Configuration with Holder and QuickConne0270-12032026-05-15
00840432200117CystoView™CystoView™ Monitor0570-04652026-05-15
00840432200308CystoView™Clamp Kit Configuration with Holder and QuickConne0270-12022026-05-15
00840432200315CystoView™Clamp Kit Configuration with QuickConnect™ Cable0270-12012026-05-15
00840432200322CystoView™Monitor with QuickConnect™ Cable0270-12002026-05-15
00879123007841GlideScope®ClearFit™ Video Baton0570-04252025-08-01
00879123008381GlideScope®ClearFit™ Hyperangle 3 Cover0574-02422025-08-01
00879123008398GlideScope®ClearFit™ Hyperangle 4 Cover0574-02432025-08-01
00879123008428GlideScope®ClearFit™ Miller 2 Cover0574-02472025-08-01
00879123008442GlideScope®ClearFit™ MAC 2 Cover0574-02442025-08-01
00879123008459GlideScope®ClearFit™ MAC 3 Cover0574-02452025-08-01
00879123008466GlideScope®ClearFit™ MAC 4 Cover0574-02462025-08-01
00879123007612GlideScope®GlideScope® Go™ 2 Monitor Configuration0270-11862025-08-01

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Primary DI, Brand, Company table
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06972084140672WiScope®Ningbo Wise Optomech Technology CorporationFAJ2026-07-28
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00848657078450AEDNATIONAL ADVANCED ENDOSCOPY DEVICES, INC.FAJ2026-07-22
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