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Transonic Systems Inc.

United States·US-MF-000008784

Last updated September 18, 2026

About

The unprecedented resolution of Transonic measurements has made Transonic synonymous with gold standard diagnostic and research measurement tools.

From the manufacturer's own website. Source

What Transonic Systems Inc. makes

Transonic Systems Inc. manufactures invasive and noninvasive vascular ultrasound systems for real-time blood flow assessment, including line-powered portable models. The company also produces thermal-dilution cardiac output units for precise hemodynamic monitoring and laser Doppler blood flowmeters for microcirculatory analysis. Additionally, it supplies clinical chemistry analysers for metabolic profiling and surgical anti-adhesion materials designed to prevent tissue adhesion during procedures.

The company’s devices are authorised under FDA 510(k) and UDI regulations in the US and listed in the EU’s eudamed registry, with classifications spanning Class I, Class II, and Class IIa. Its portfolio is regulated according to regional medical device standards, ensuring compliance with invasive, diagnostic, and implantable product requirements.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
United States
Address
34, Dutch Mill Rd., Ithaca, United States
Facebook
—
Phone
607-257-5300
PRRC Contact
Cornelis Drost
EUDAMED SRN
US-MF-000008784
FDA FEI Number
—
DUNS Number
101317451

Catalogue (713)

Page 15 of 15
DeviceModel / ReferenceRegistriesClassStatus
Tubing Flowsensors H7FX
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors HQD5XL
EUDAMEDFDA UDI
Class IIaActive
Standard FlowXL Meter with AdvancedFlow Software HT520AF
EUDAMED
Class IIaActive
Tubing Flowsensors HS3XL
EUDAMED
Class IIaActive
Tubing Flowsensors HS10XL
EUDAMED
Class IIaActive
Tubing Flowsensors HQD11XL
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors HS4XL
EUDAMED
Class IIaActive
Tubing Flowsensors HQD7XL
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors HQD8XL
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors H6FX
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors H5XL
EUDAMEDFDA UDI
Class IIaActive
Tubing Flowsensors HS8XL
EUDAMED
Class IIaActive
Tubing Flowsensors H7XL
EUDAMEDFDA UDI
Class IIaActive

Related Companies

Authorised Representatives

Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Recalls (11)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Transonic Systems Inc. has 11 FDA recall records, all initiated between July 27, 2015, and February 15, 2018, with all records marked as terminated. The reasons cited include concerns about the sterility of a device, stating there is a potential for an increased risk of infection, and software defects in blood flow probes, specifically programming errors causing incorrect readings when connected to flow meters.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Feb 15, 2018Z-1776-2018—terminated

The sterility of the device cannot be assured. There is a potential for an increased risk of infection.

Jul 27, 2015Z-2725-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2720-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2728-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2721-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2723-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2722-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2727-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2726-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2729-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.

Jul 27, 2015Z-2724-2015—terminated

Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.