Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032577207

FEI Number

3032577207

Entity Name

POSITRIGO AG

City/State/Country

Zurich, CH

Establishment Address

Technoparkstrasse 1, Zurich 8005, CH

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Positrigo AG (Owner Number: 10091382)

Owner / Operator Contact Address

Technoparkstrasse 1, Zurich, CH-ZH 8005, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241751

PMA Number

N/A

All Registered Proprietary Names

NeuroLF (Basic) NeuroLF (Pro) NeuroLF (Advanced) NeuroLF Seat

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KPS	System, Tomography, Computed, Emission	Radiology	Class 2	892.1200	2024-09-12

Official Correspondent

Jannis Fischer

US Agent Details

Brian Oswald Business: Positrigo Inc. Email: usa@positrigo.com Phone: (305) 9234283

Related Public Records

Same Entity

Positrigo AG

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
K033956	Is2 Research, Inc.	MOBILE SINGLE CIRCULAR CAMERA (MSC) & MOBILE DIGITAL CARDIAC CAMERA (MDCC)	2004-01-20
K923309	GE Medical Systems	ARGUS PET SYSTEM	1992-09-29
K101768	Miegmbh	MIE SCINTRON GAMMA CAMERA SYSTEMS	2010-10-05

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2016	Toshiba American Medical Systems Inc	2	Celesteion PCA-9000A/2 PET/CT System
Z-0012-05	General Electric Med Systems LLC	2	Emission Computed Tomography System. Including Model numbers: 2200967, ASM001080, ASM001083, ASM001092, ASM001099, ASM000085, 10036800109, and Varicam.
Z-0013-2007	Philips Medical Systems (Cleveland) Inc	2	Nuclear medicine systems: Gemini 16, Model 4535 679 28961. Gemini GXL, Models # 4535 679 71891, #4535 679 75681, #4535 679 75691. Precedence, Model #2169 -3000A, #2169-3001A, #2169-3002A, and 2169-3003A. PET/CT Computed tomography systems.
Z-0014-2007	Philips Medical Systems (Cleveland) Inc	2	Brilliance(a) CT 6 slice, Model #4535 670 73191. Brilliance(a) CT 10 Slice, Model 4535 670 73181. Brilliance 16 Slice, Model #4535 670 78851. Brilliance CT 16 Power, Model #4535 670 23331. Brilliance CT 40 Slice, Model #4550 110 04011. Brilliance CT Big Bore, Model #4535 670 88051. Computed tomography systems.
Z-0024-2014	GE Healthcare, LLC	2	GE PET Discovery 610, PET Discovery 710. Intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging.

Similar Registrations

Registration Number	Establishment Name	Location
3009136051	CEDARS SINAI MEDICAL CENTER	Los Angeles, CA, US
9614698	CANON INC.	OTAWARA-SHI Tochigi, JP
3011950073	United Imaging Healthcare North America, Inc	Houston, TX, US
3008962177	GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.	Valencia, ES
1423253	SIEMENS MEDICAL SOLUTIONS USA, INC.	Hoffman Estates, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032577207. Last updated year: 2026. Please use registration number 3032577207 when referencing this establishment in official correspondence.