Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 12 of 15
DeviceModel / ReferenceRegistriesClassStatus
Transonic HQN1.5MB
FDA UDI
Class IIActive
Transonic HQC7XL
FDA UDI
Class IIUnknown
Transonic HQE28AU
FDA UDI
Class IIUnknown
Transonic HQE14FSB
FDA UDI
Class IIUnknown
Transonic HQC2FSB
FDA UDI
Class IIUnknown
Transonic HQN3FME
FDA UDI
Class IIActive
Transonic HQC2XL
FDA UDI
Class IIUnknown
Transonic HQN1.5MR
FDA UDI
Class IIActive
Transonic HT312
FDA UDI
Class IIUnknown
Transonic HQD32AU
FDA UDI
Class IIUnknown
Transonic HQF20AU
FDA UDI
Class IIActive
Transonic HQF8FTV
FDA UDI
Class IIUnknown
Transonic HQF8AU
FDA UDI
Class IIActive
Transonic H12AUL-5
FDA UDI
Class IIActive
Transonic HQF1.5FD
FDA UDI
Class IIActive
Transonic ABLPHDI
FDA UDI
Class IIActive
Transonic HQD10FTV
FDA UDI
Class IIUnknown
Transonic HQD1.5MR
FDA UDI
Class IIUnknown
Transonic HQD2XLP
FDA UDI
Class IIUnknown
Transonic HQN10FME
FDA UDI
Class IIUnknown
Transonic HQE3MR-S
FDA UDI
Class IIActive
Transonic ADT1010-40
FDA UDI
Class IIActive
Transonic HQD6FMV
FDA UDI
Class IIActive
Transonic HQD12XL
FDA UDI
Class IIUnknown
Transonic HQE2FME
FDA UDI
Class IIUnknown
Transonic HQD3MR
FDA UDI
Class IIActive
Transonic HQN4FME
FDA UDI
Class IIUnknown
Transonic HQG4MB-S
FDA UDI
Class IIActive
Transonic HCS3002
FDA UDI
Class IIUnknown
Transonic HQF3FD
FDA UDI
Class IIActive
Transonic HQC3MP
FDA UDI
Class IIUnknown
Transonic HQN4MR-S
FDA UDI
Class IIUnknown
Transonic H6AUL
FDA UDI
Class IIUnknown
Transonic HQE10FTE
FDA UDI
Class IIUnknown
Transonic HQE8FME
FDA UDI
Class IIUnknown
Transonic H36AUL-5
FDA UDI
Class IIUnknown
Transonic HQE3MU
FDA UDI
Class IIUnknown
Transonic HQD5XL-M8
FDA UDI
Class IIUnknown
Transonic HQD3P
FDA UDI
Class IIUnknown
Transonic HQC10MP
FDA UDI
Class IIUnknown
Transonic HQN1.5MR
FDA UDI
Class IIUnknown
Transonic HQD8FTE
FDA UDI
Class IIUnknown
Transonic HQF16AU
FDA UDI
Class IIUnknown
Transonic HQC1.5FMV
FDA UDI
Class IIUnknown
Transonic ADT1002-10
FDA UDI
Class IIUnknown
Transonic HQF8FME
FDA UDI
Class IIActive
Transonic HQD2FMV
FDA UDI
Class IIUnknown
Transonic HCS3021-5
FDA UDI
Class IIUnknown
Transonic HQF2FMV
FDA UDI
Class IIUnknown
Transonic HQC10AU
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.