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Data / Medical devices / Canada / Labtician Ophthalmics, Inc.

Labtician Ophthalmics, Inc.: FDA-registered device maker in OAKVILLE Ontario, Canada, 2 510(k) clearances

Labtician Ophthalmics, Inc. is registered with the FDA (registration 9612327) in OAKVILLE Ontario, Canada. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 8, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9612327
FEI number
3002807445
Address
2140 Winston Park DR., Unit 6, OAKVILLE Ontario, Canada, L6H 5V5
Owner or operator
LABTICIAN OPHTHALMICS, INC. (8022288)
Roles
Manufacturer, Repackager or relabeler
First device listed
April 20, 1999
Registered through
2026
Brand names listed
LABTICIAN LID LOAD ADHESIVE STRIPS, LSO QUICKSET, LabVit Kit, Labtician Lid Load Gold Eyelid Weight Implant, Labtician Retinal Implant

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 8, 1999K983607LABTICIAN LID LOAD GOLD EYELID WEIGHT IMPLANTSMMLSubstantially EquivalentLabtician Ophthalmics, Inc.accessdata.fda.gov
February 26, 1988K875014LABTICIAN RETINAL IMPLANTSHQJSubstantially EquivalentLabtician Products, Inc.accessdata.fda.gov

Compare with other makers

Updated January 8, 1999. 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.