TREVI TECHNOLOGY

FDA Device Registration & Listing · Columbus, OH, US · Registration 3005771344

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005771344
FEI Number
3005771344
Entity Name
TREVI TECHNOLOGY
City/State/Country
Columbus, OH, US
Establishment Address
2451 Marblevista Blvd, Columbus, OH 43204, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Trevi Technology (Owner Number: 10041846)
Owner / Operator Contact Address
2451 Marblevista Blvd, Columbus, OH 43204, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Manual PD Meter Ibex Lensmeter BIO Ibex Acuity Chart Ibex Motorized Instrument Table Slit Lamp Microscope Manual Tonometer Ibex Manual Refractor IBEX Forceps PLC-8000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLH Pupillometer, Manual Ophthalmic Class 1 886.1700 2015-08-19
HLM Instrument, Measuring, Lens, Ac-Powered Ophthalmic Class 1 886.1425 2016-03-21
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2015-08-19
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2015-08-19
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2016-03-30
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 2016-03-30
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2015-08-19
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2015-08-19
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2016-03-21
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2023-01-24
HOS Projector, Ophthalmic Ophthalmic Class 1 886.1680 2023-07-24

Official Correspondent

Kevin Intrieri

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Trevi Technology
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K870750 Keeler Instruments, Inc. KEELER PULSAIR NON CONTACT TONOMETER 1987-03-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2018 Optovue, Inc. 2
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional, and three dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue with Normative Database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0010-2018 Optovue, Inc. 2
iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue 500 with normative database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue 500 with normative database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.

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3011898560 BEIJING HONGDEE CORPORATION Beijing, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005771344. Last updated year: 2026. Please use registration number 3005771344 when referencing this establishment in official correspondence.
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