FDA.reportPublic FDA data

SonoVision

Primary DI
00860001239300
Brand
SonoVision
Company
Tissue Differentiation Intelligence LLC
Model
100039
Device description
SonoVision Accessory Kit
Published
2022-11-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FFORetractor, Self-Retaining
FZXGuide, Surgical, Instrument
GADRetractor
HTDForceps
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FFORetractor, Self-RetainingGastroenterology, Urology1
FZXGuide, Surgical, InstrumentGeneral, Plastic Surgery1
GADRetractorGeneral, Plastic Surgery1
HTDForcepsGeneral, Plastic Surgery1
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00860001239300PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00860001239300008600012393008600012393000860001239300

GMDN Terms#

Term, Definition table
TermDefinition
Interventional radiology percutaneous-access kit, reusableA collection of various instruments/devices (e.g., introducer sheath, dilator, guides, cannula, needle, angiographic catheter) intended to be used for percutaneous body-access to facilitate a radiological image-guided interventional radiology or surgical procedure [e.g., bile duct biopsy, percutaneous transhepatic cholangiogram, non-vascular drainage procedures, ultrasound-guided spinal surgery]. Some types are designed to function as a channel to facilitate the introduction of radiological image guidance devices (e.g., ultrasound probe/transducer) [not included]. It does not contain pharmaceuticals. This is a reusable device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Handle with care
Special Storage Condition, Specify00Keep Dry

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
305-351-2011customerservice@tissueintel.com

Regulatory Flags#

DUNS number
081327336
Device count
1
Premarket exempt
true
Serial number
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00860001239324SonoVision1000212022-12-08
00860001239331SonoVision1000222022-12-08
00860001239362SonoVision1000302022-12-08
00860001239379SonoVision1000332022-12-08
00860001239386SonoVision1000342022-12-08
00860001239348Beluga11000052022-03-03
00860001239355SonoVision1000092022-03-03

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776437220MillenniumAvalign Technologies, Inc.HTD2026-10-28
00190776439811MilleniumAvalign Technologies, Inc.GAD2026-10-28
10888857615779K2M General InstrumentsVB Spine LLCLXH2026-10-28
B382SD902949100Surgical DirectSurgical Direct, Inc.HTD2026-10-28
B382SD907310080Surgical DirectSurgical Direct, Inc.GAD2026-10-28
B382SD9141781200Surgical DirectSurgical Direct, Inc.GAD2026-10-28
B382SD91417912190Surgical DirectSurgical Direct, Inc.GAD2026-10-28
M739193990906Non-Modular Convex TrialCAPTIVA SPINE, INC.LXH2026-10-28
M739193996906Non-Modular Lordotic Trial AssemblyCAPTIVA SPINE, INC.LXH2026-10-28
M739243999005SG Implant Driver-SCAPTIVA SPINE, INC.LXH2026-10-28
M739985202229Marking PinCAPTIVA SPINE, INC.LXH2026-10-28
M739985202229Marking PinCAPTIVA SPINE, INC.FZX2026-10-28
M739985203229Marking PinCAPTIVA SPINE, INC.FZX2026-10-28
M739985203229Marking PinCAPTIVA SPINE, INC.LXH2026-10-28
00192896123984Trepsat Flap Dissecting ForcepsSONTEC INSTRUMENTS, INC.HTD2026-10-27
00192896123991Trepsat Flap Dissecting ForcepsSONTEC INSTRUMENTS, INC.HTD2026-10-27
00192896124004Trepsat Flap Dissecting ForcepsSONTEC INSTRUMENTS, INC.HTD2026-10-27
00724995264949Snowden-PencerSTERIS Deutschland GmbHHTD2026-10-27
00810055525164NON NAVIGATED STYLET-OBTURATOR ASSEMBLYSi-Bone Inc.LXH2026-10-27
00810055525188CANNULATED PROBE IMPACTION CAP ASSEMBLYSi-Bone Inc.LXH2026-10-27
00810055525195CANNULATED PROBE HANDLE ASSEMBLYSi-Bone Inc.LXH2026-10-27
00810055525218GRANITE CANNULATED PROBE SHAFTSi-Bone Inc.LXH2026-10-27
00889024702233OsseoFitZimmer, Inc.LXH2026-10-27
00889024702240OsseoFitZimmer, Inc.LXH2026-10-27
00889024702295OsseoFitZimmer, Inc.FZX2026-10-27
00889024702301OsseoFitZimmer, Inc.FZX2026-10-27
00889024702479OsseoFitZimmer, Inc.LXH2026-10-27
04250337119210Counter Pusher, greenJoimax GmbHFZX2026-10-27
04250337119227Counter Pusher, yellowJoimax GmbHFZX2026-10-27
04250337119234Counter Pusher, redJoimax GmbHFZX2026-10-27