MEDIVIS, INC.

FDA Device Registration & Listing · New York, NY, US · Registration 3015536273

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
3015536273
FEI Number
3015536273
Entity Name
MEDIVIS, INC.
City/State/Country
New York, NY, US
Establishment Address
174 5th Ave Fl 2, New York, NY 10010, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MEDIVIS, Inc. (Owner Number: 10060771)
Owner / Operator Contact Address
174 5th ave, Floor 2, New York, NY 10010, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Cranial Navigation System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HAW Neurological Stereotaxic Instrument Neurology Class 2 882.4560 2025-12-13

Official Correspondent

Amy Lynn

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDIVIS, 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
K010427 Walter Lorenz Surgical, Inc. LORENZ FIDUCAIL SCREW 2001-03-15
K812744 Progress Mankind Technology LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER 1981-12-03
K092467 Brainlab AG VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED 2010-05-06
K031454 Biomet, Inc. ACUMEN SURGICAL NAVIGATION SYSTEM 2004-07-08

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2012 Medtronic Navigation, Inc 2
Probe, Tactile, Left, ASM, Long, Part #962009S, Medtronic Navigation, Louisville, CO 80027. Trackable hand held instruments used in spine surgeries for preparation of the pedicle. These instruments are used in conjunction with the Medtronic Navigation StealthStation platform and various software applications.
Z-0002-2012 Medtronic Navigation, Inc 2
Probe, Tactile, Right, ASM, Long, Part #962011S, Medtronic Navigation, Louisville, CO 80027. Trackable hand held instruments used in spine surgeries for preparation of the pedicle. These instruments are used in conjunction with the Medtronic Navigation StealthStation platform and various software applications.
Z-0005-2007 Stryker Instruments Div. of Stryker Corporation 2
Stryker Navigation System, eNlite System with Dell laptop computer model D800, Stryker # 7700-300-000.
Z-0006-2007 Stryker Instruments Div. of Stryker Corporation 2
Stryker Navigation System Remote Planning Stations with Dell laptop computer model D800, Stryker # 7700-010-000 and 6000-300-000.
Z-0007-2007 Stryker Instruments Div. of Stryker Corporation 2
Stryker Navigation System Dell Model D800 laptop computers (only), Stryker # 7700-309-010 and 6000-200-064.

Similar Registrations

Registration Number Establishment Name Location
3002743211 NORTHERN DIGITAL, INC. WATERLOO Ontario, CA
3009108888 RENISHAW MAYFIELD Chassieu Rhone, FR
3018708317 MAGNUS MEDICAL INC. Burlingame, CA, US
2434444 NEURODYNAMICS, INC. Manhattan, NY, US
3017004815 RENISHAW NEURO SOLUTIONS LTD Wotton-under-Edge Gloucestershire, GB
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015536273. Last updated year: 2026. Please use registration number 3015536273 when referencing this establishment in official correspondence.
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