Data / Medical devices / United States / Trevi Technology

Trevi Technology: FDA-registered device maker in Columbus, OH, United States, 3 510(k) clearances

Name: Trevi Technology FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Trevi Technology is registered with the FDA (registration 3005771344) in Columbus, OH, United States. It lists 15 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 9, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3005771344
Address: 2451 Marblevista Blvd, Columbus, OH, United States, 43204
Owner or operator: Trevi Technology (10041846)
Roles: Repackager or relabeler
First device listed: August 19, 2015
Registered through: 2026
Brand names listed: BIO, Cannula, IBEX Forceps, Ibex Acuity Chart, Ibex Lensmeter, Ibex Manual Refractor, Ibex Motorized Instrument Table, Keratometer and more

Devices it lists

Device	Product code	Class	Role	Source
Biomicroscope, Slit-Lamp, Ac-Powered	HJO	2	Repackager or relabeler	accessdata.fda.gov
Cannula, Ophthalmic	HMX	1	Repackager or relabeler	accessdata.fda.gov
Chart, Visual Acuity	HOX	1	Repackager or relabeler	accessdata.fda.gov
Forceps, Ophthalmic	HNR	1	Repackager or relabeler	accessdata.fda.gov
Instrument, Measuring, Lens, Ac-Powered	HLM	1	Repackager or relabeler	accessdata.fda.gov
Keratoscope, Ac-Powered	HLQ	1	Repackager or relabeler	accessdata.fda.gov
Ophthalmoscope, Ac-Powered	HLI	2	Repackager or relabeler	accessdata.fda.gov
Ophthalmoscope, Battery-Powered	HLJ	2	Repackager or relabeler	accessdata.fda.gov
Projector, Ophthalmic	HOS	1	Repackager or relabeler	accessdata.fda.gov
Pupillometer, Manual	HLH	1	Repackager or relabeler	accessdata.fda.gov
Refractometer, Ophthalmic	HKO	1	Repackager or relabeler	accessdata.fda.gov
Refractor, Manual, Non-Powered, Including Phoropter	HKN	1	Repackager or relabeler	accessdata.fda.gov
Scissors, Ophthalmic	HNF	1	Repackager or relabeler	accessdata.fda.gov
Table, Instrument, Powered, Ophthalmic	HRJ	1	Repackager or relabeler	accessdata.fda.gov
Tonometer, Ac-Powered	HKX	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
February 9, 2011	K110205	AAIO-7, AAIO WIRLESS	HLI	Substantially Equivalent	Appasamy Associates	accessdata.fda.gov
July 31, 2008	K082031	APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES	HJO	Substantially Equivalent	Appasamy Associates	accessdata.fda.gov
April 24, 2003	K023676	APPLANATION TONOMETER	HKX	Substantially Equivalent	Optilasa, S.L.	accessdata.fda.gov

Compare with other makers

Updated February 9, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.