ACCUTOME, INC.

FDA Device Registration & Listing · Malvern, PA, US · Registration 2521877

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
2521877
FEI Number
2521877
Entity Name
ACCUTOME, INC.
City/State/Country
Malvern, PA, US
Establishment Address
3222 Phoenixville Pike, Malvern, PA 19355, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
ACCUTOME, INC. (Owner Number: 2521877)
Owner / Operator Contact Address
3222 Phoenixville Pike, --, Malvern, PA 19355, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stimuli CVT Roland Darkadoptometer PDT Kit Generic GENERIC OPHTHALMIC RING

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2021-02-19
HNC Specula, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2021-02-19
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2021-02-19
HXB Probe Orthopedic Class 1 888.4540 1999-02-16
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2009-02-25
HNB Spoon, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HJW Adaptometer (Biophotometer) Ophthalmic Class 1 886.1050 2009-05-11
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2008-12-16
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2021-02-19
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2021-02-19
OJK Eye Tray Ophthalmic Class 2 886.4790 2011-04-22
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2014-04-25
HNQ Hook, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2010-02-02
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2021-02-19
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2013-02-08
ITX Transducer, Ultrasonic, Diagnostic Radiology Class 2 892.1570 2013-02-08
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2015-11-30
ITX Transducer, Ultrasonic, Diagnostic Radiology Class 2 892.1570 2015-11-30
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2021-02-19
PJZ Camera, Ophthalmic, General-Use Ophthalmic Class 2 886.1120 2020-11-30
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2021-02-19
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2021-02-19
JYJ Gauge, Measuring Ear, Nose, Throat Class 1 874.4420 1992-07-29
HMX Cannula, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HKL Retinoscope, Ac-Powered Ophthalmic Class 2 886.1780 2021-02-19
GZX Instrument, Microsurgical Neurology Class 1 882.4525 2010-02-02
HOE Caliper, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
HRN Unit, Cryophthalmic, Ac-Powered Ophthalmic Class 2 886.4170 2021-02-19
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2020-02-03
HON Perimeter, Manual Ophthalmic Class 1 886.1605 1999-02-16
HNF Scissors, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
GAR Suture, Nonabsorbable, Synthetic, Polyamide General, Plastic Surgery Class 2 878.5020 2007-02-08
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 1999-02-18
HND Spatula, Ophthalmic Ophthalmic Class 1 886.4350 1999-02-16
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2007-02-08
GDL Needle, Suturing, Reusable General, Plastic Surgery Class 1 878.4800 2007-02-08
HNX Depressor, Orbital Ophthalmic Class 1 886.4350 1999-02-16
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2008-12-16
ITX Transducer, Ultrasonic, Diagnostic Radiology Class 2 892.1570 2008-12-16
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2010-08-09
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2021-02-19
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2021-02-19
HRN Unit, Cryophthalmic, Ac-Powered Ophthalmic Class 2 886.4170 2021-02-19
HNW Dilator, Lachrymal Ophthalmic Class 1 886.4350 1999-02-16
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 1992-07-29
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2021-02-19
HJM Transilluminator, Ac-Powered Ophthalmic Class 2 886.1945 2021-02-19
HNH Ring, Ophthalmic (Flieringa) Ophthalmic Class 1 886.4350 2000-04-24

Official Correspondent

Claudia Hill

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ACCUTOME, INC.
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
K882805 Coopervision-Cilco CILCO VILLASENOR PACHYMETER 1988-08-12
K791040 Shimadzu Corp. SECTOR SCANNER, SDU-100, COMPUTERIZED 1979-10-04
K162372 Qt Ultrasound, LLC QT Ultrasound Breast Scanner-1 2017-06-06
K930964 Acuson Corp. ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE) 1994-10-26

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.
Z-0003-2011 Verathon, Inc. 2
BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600 with AortaScan Mode is a user-selectable, dual-function ultrasound device that projects ultrasound energy either into the lower abdomen to obtain an image of the bladder for measuring bladder volume, or into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements.
Z-0004-2011 Verathon, Inc. 2
AortaScan AMI 9700 The AortaScan AMI 9700 is an ultrasound device that projects ultrasound energy into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements
Z-0005-2011 Verathon, Inc. 2
BladderScan BVM 9500 The BladderScan BVM 9500 is intended to project ultrasound energy through the lower abdomen to obtain an image of the bladder and measure urinary bladder volume and mass noninvasively.
Z-0027-2014 SonoSite, Inc. 2
P21x/5-1 MHz transducer, Part Number P07698-23 Product Usage: The P21x/5-1 MHz phased array transducer is designed for cardiac, abdominal and obstetric, TCD and orbital exams. It supports 2D with SonoMB Multi Beam Technology and Auto Gain capabilities, SonoHD Imaging Technology, Tissue Harmonic Imaging, M-Mode, Velocity Color Flow Doppler, Color Power Doppler (CDP), Pulsed Wave (PW), TDI Pulsed Wave, and Continuous Wave Doppler.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2521877. Last updated year: 2026. Please use registration number 2521877 when referencing this establishment in official correspondence.
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