PRECISION OPTICS CORP.

FDA Device Registration & Listing · GARDNER, MA, US · Registration 1222616

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
1222616
FEI Number
1000120916
Entity Name
PRECISION OPTICS CORP.
City/State/Country
GARDNER, MA, US
Establishment Address
22 E Broadway, GARDNER, MA 01440, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PRECISION OPTICS CORP. (Owner Number: 9001379)
Owner / Operator Contact Address
22 EAST BROADWAY, --, Gardner, MA 01440, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Heartlight System RetCam Envision Otoscan Spotlight Access System Hydros Robotic System Laryngostroboscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2017-07-13
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2026-03-30
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 1998-09-21
GZT Retractor, Self-Retaining, For Neurosurgery Neurology Class 2 882.4800 2013-01-22
FSQ Light, Surgical, Instrument General, Plastic Surgery Class 2 878.4580 2013-01-22
PZP Fluid Jet Removal System General, Plastic Surgery Class 2 876.4350 2026-03-30
EQL Laryngostroboscope Ear, Nose, Throat Class 1 874.4750 2011-03-15

Official Correspondent

Troy Evangelista

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRECISION OPTICS CORP.
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
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08

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 1222616. Last updated year: 2026. Please use registration number 1222616 when referencing this establishment in official correspondence.
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