FDA.reportPublic FDA data

FLASH Flex Aorto-Ostial Angioplasty System

Primary DI
00810219610118
Brand
FLASH Flex Aorto-Ostial Angioplasty System
Company
Verge Medical, Inc.
Model
FF50A
Catalog number
FF50A
Device description
FLASH Flex Aorto-Ostial Angioplasty System, 5.0mm x 12mm
Published
2026-05-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LOXCatheters, Transluminal Coronary Angioplasty, Percutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LOXCatheters, Transluminal Coronary Angioplasty, PercutaneousCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K254022000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K254022000FLASH Flex™ Aorto-Ostial Angioplasty SystemVerge Medical, Inc.2026-04-02LOX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810219610118PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810219610118008102196101188102196101180810219610118

GMDN Terms#

Term, Definition table
TermDefinition
Coronary angioplasty balloon catheter, basicA flexible tube designed for percutaneous transluminal coronary angioplasty (PTCA) to dilate a stenotic coronary artery by controlled inflation of a distensible balloon(s) at its distal tip. It is typically available as: 1) an over-the-wire (OTW) type that has a double or triple-lumen, one for the guidewire and one or two for single- or double-balloon inflation; and 2) a rapid exchange (RX) type with a single-lumen. It is available in various sizes for the dilatation of small, narrowed, or obstructed coronary arteries or bypass grafts. It may also be intended for pre- or post-dilatation of a balloon-expandable stent (not included) in the coronary arteries. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Balloon Diameter0
Balloon Length0
Catheter Length0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in a dry location at room temperature.

Contacts#

Phone, Email table
PhoneEmail
1-844-352-7411customerservice@vergemedical.com

Regulatory Flags#

DUNS number
078708447
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810219610071FLASH Flex Aorto-Ostial Angioplasty SystemFF30AFF30A2026-05-22
00810219610088FLASH Flex Aorto-Ostial Angioplasty SystemFF35AFF35A2026-05-22
00810219610095FLASH Flex Aorto-Ostial Angioplasty SystemFF40AFF40A2026-05-22
00810219610101FLASH Flex Aorto-Ostial Angioplasty SystemFF45AFF45A2026-05-22
M917RVHD0RoVo Mechanical Thrombectomy SystemRVHDRVHD2026-02-06
M917RVHD1RoVo Mechanical Thrombectomy SystemRVHDRVHD2026-02-06
M917VRG7513B30RoVo Mechanical Thrombectomy SystemVRG7513B3VRG7513B32026-02-06
M917OTW7017BA0FLASH Ostial System OTWOTW7017BAOTW7017BA2016-09-22
M917OAB6019BA0FLASH Ostial SystemOAB6019BAOAB6019BA2016-09-22
M917OAB7019BA0FLASH Ostial SystemOAB7019BAOAB7019BA2016-09-22
M917OCB4014BA0FLASH Ostial SystemOCB4014BAOCB4014BA2016-09-22
M917OCB4514BA0FLASH Ostial SystemOCB4514BAOCB4514BA2016-09-22
M917OCB5019BA0FLASH Ostial SystemOCB5019BAOCB5019BA2016-09-22
M917OAB6014BA0FLASH Ostial SystemOAB6014BAOAB6014BA2016-09-22
M917OTW6012BA0FLASH Ostial System OTWOTW6012BAOTW6012BA2016-09-22
M917OTW7012BA0FLASH Ostial System OTWOTW7012BAOTW7012BA2016-09-22
M917OCB3008BA0FLASH MINI Ostial SystemOCB3008BAOCB3008BA2016-09-22
M917OCB3508BA0FLASH MINI Ostial SystemOCB3508BAOCB3508BA2016-09-22
M917OCB4008BA0FLASH MINI Ostial SystemOCB4008BAOCB4008BA2016-09-22
M917OCB4508BA0FLASH MINI Ostial SystemOCB4508BAOCB4508BA2016-09-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00810219610071FLASH Flex Aorto-Ostial Angioplasty SystemVerge Medical, Inc.LOX2026-05-22
00810219610088FLASH Flex Aorto-Ostial Angioplasty SystemVerge Medical, Inc.LOX2026-05-22
00810219610095FLASH Flex Aorto-Ostial Angioplasty SystemVerge Medical, Inc.LOX2026-05-22
00810219610101FLASH Flex Aorto-Ostial Angioplasty SystemVerge Medical, Inc.LOX2026-05-22
06971591769062Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769079Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769086Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769093Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769109Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769116Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769123Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769130Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
06971591769147Selebrek PTCA Balloon Dilatation CatheterKossel Medtech (Suzhou) Co., Ltd.LOX2026-04-19
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00763000877071SPRINTER® LEGENDMEDTRONIC, INC.LOX2025-09-19
00763000877088SPRINTER® LEGENDMEDTRONIC, INC.LOX2025-09-19
00763000877095SPRINTER® LEGENDMEDTRONIC, INC.LOX2025-09-19
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