FORUS HEALTH PVT.LTD.,

FDA Device Registration & Listing · Bengaluru Karnataka, IN · Registration 3012162565

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
3012162565
FEI Number
3012162565
Entity Name
FORUS HEALTH PVT.LTD.,
City/State/Country
Bengaluru Karnataka, IN
Establishment Address
No. 8, 27th Cross Rd, Banashankari Stage II, Banashankari, Bengaluru Karnataka 560070, IN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FORUS HEALTH PVT.LTD., (Owner Number: 10050919)
Owner / Operator Contact Address
No. 8, 27th cross,, Banashankari 2nd stage, Bengaluru, IN-KA 560070, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

G5 Vision Screener 3nethra SL5-1000 3nethra SL5-1000 Pro 3nethra neo 3nethra neo HD 3nethra neo HD FA 3nethra classic 3nethra classic HD 3nethra classic 6.4 3nethra classic+ 3nethra pico 3nethra ultima

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMF Photorefractor Ophthalmic Class 2 886.1120 2026-05-13
PUE Biomicroscope, Slit-Lamp, Ac-Powered, Exempt Ophthalmic Class 2 886.1850 2025-06-10
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2019-01-14
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2025-08-18
PJZ Camera, Ophthalmic, General-Use Ophthalmic Class 2 886.1120 2016-01-18

Official Correspondent

No official correspondent registered.

US Agent Details

Donny Thomas Business: Forus Health, Inc. Email: donny@forushealth.com Phone: (703) 7241646

Related Public Records

Same Entity

FORUS HEALTH PVT.LTD.,
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
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 3012162565. Last updated year: 2026. Please use registration number 3012162565 when referencing this establishment in official correspondence.
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