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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 9 of 15
DeviceModel / ReferenceRegistriesClassStatus
Transonic H4AUL
FDA UDI
Class IIUnknown
Transonic HCM101
FDA UDI
Class IIActive
Transonic H16AUL
FDA UDI
Class IIUnknown
Transonic HQD14XL
FDA UDI
Class IIUnknown
Transonic HQF4FMV
FDA UDI
Class IIUnknown
Transonic HQN4MB-S
FDA UDI
Class IIActive
Transonic HQD2P
FDA UDI
Class IIActive
Transonic HQE1MU
FDA UDI
Class IIUnknown
Transonic HQF1MU
FDA UDI
Class IIActive
Transonic HQF1.5FMV
FDA UDI
Class IIUnknown
Transonic HQC6MP
FDA UDI
Class IIActive
Transonic H24AUL-5
FDA UDI
Class IIUnknown
Transonic HQC6FTE
FDA UDI
Class IIUnknown
Transonic HQD3MR
FDA UDI
Class IIUnknown
Transonic HQN4FME
FDA UDI
Class IIActive
Transonic HQC36AU
FDA UDI
Class IIUnknown
Transonic HQN3MR-S
FDA UDI
Class IIActive
Transonic HQC1.5FMC
FDA UDI
Class IIUnknown
Transonic HQF3FMV
FDA UDI
Class IIUnknown
Transonic H10AUL-5
FDA UDI
Class IIUnknown
Transonic HQN2MB
FDA UDI
Class IIUnknown
Transonic HQF3MR
FDA UDI
Class IIActive
Transonic HQD12FSB
FDA UDI
Class IIUnknown
Transonic HQF1MU
FDA UDI
Class IIUnknown
Transonic HQF32AU
FDA UDI
Class IIActive
Transonic HQD28AU
FDA UDI
Class IIUnknown
Transonic H20AUL-5
FDA UDI
Class IIActive
Transonic HQF4MR-S
FDA UDI
Class IIUnknown
Transonic HQF1.5FSB
FDA UDI
Class IIUnknown
Transonic HQC4FTV
FDA UDI
Class IIUnknown
Transonic HQC4FME
FDA UDI
Class IIUnknown
Transonic HQD4XL-M6
FDA UDI
Class IIUnknown
Transonic HQF6MR-S
FDA UDI
Class IIUnknown
Transonic HQD2FSB
FDA UDI
Class IIUnknown
Transonic HQN3MB
FDA UDI
Class IIUnknown
Transonic HQN3MR
FDA UDI
Class IIUnknown
Transonic HQD3P
FDA UDI
Class IIActive
Transonic HQN1.5MB
FDA UDI
Class IIUnknown
Transonic HQN10FME
FDA UDI
Class IIActive
Transonic HQE0.7MU
FDA UDI
Class IIUnknown
Transonic HQF10FME
FDA UDI
Class IIUnknown
Transonic HQF2P
FDA UDI
Class IIUnknown
Transonic H20AUL
FDA UDI
Class IIUnknown
Transonic HCS3011
FDA UDI
Class IIUnknown
Transonic HQF1.5FMC
FDA UDI
Class IIUnknown
Transonic HQE4FME
FDA UDI
Class IIUnknown
Transonic HFW1000
FDA UDI
Class IIActive
Transonic HQC6FME
FDA UDI
Class IIUnknown
Transonic HQF3FD
FDA UDI
Class IIUnknown
Transonic BLF21
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

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.