TearScience, Inc.

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3008169506

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
3008169506
FEI Number
3008169506
Entity Name
TearScience, Inc.
City/State/Country
Milpitas, CA, US
Establishment Address
510 Cottonwood Drive, Milpitas, CA 95035, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Johnson & Johnson Surgical Vision, Inc. (Owner Number: 10053607)
Owner / Operator Contact Address
31 Technology Dr., Suite 200, Irvine, CA 92618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Meibomian Gland Evaluator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOE Caliper, Ophthalmic Ophthalmic Class 1 886.4350 2018-11-18
ORZ Eyelid Thermal Pulsation System Ophthalmic Class 2 886.5200 2018-11-18
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2018-11-18
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2018-11-18
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2018-12-12
ORZ Eyelid Thermal Pulsation System Ophthalmic Class 2 886.5200 2019-11-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Johnson & Johnson Surgical Vision, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005675890 OptiMedica Corp. Milpitas, CA, US
3004750704 AMO UPPSALA AB UPPSALA, SE
3011714173 AMO (HANGZHOU PARK) WAREHOUSE Hangzhou Zhejiang, CN
9614546 AMO GRONINGEN BV GRONINGEN, NL
3004178847 AMO (HANGZHOU) CO., LTD. HANGZHOU Zhejiang, CN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2018 Optovue, Inc. 2
iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging device which is suitable for photographing, displaying and storing images of the retina and external areas of the eye to be evaluated under non-mydriatic conditions. The iCam takes digital images of the posterior and external structures of the eye without the use of a mydriatic agent and is intended for use as an aid to clinicians in the evaluation, diagnosis and documentation of ocular health. iCam provides images only and does not provide any diagnostic, pathological analysis or classification of ocular health or disease. AND iVue with Normative Database (K121739) - The iVue is a noncontact, high resolution optical coherence tomography system intended for in vivo imaging, axial cross-sectional, 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 comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008169506. Last updated year: 2026. Please use registration number 3008169506 when referencing this establishment in official correspondence.
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