Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027339477

FEI Number

3027339477

Entity Name

MEDIVEST GROUP

City/State/Country

Dinnington East Riding of Yorkshire, GB

Establishment Address

unit 8, Kingfisherway, Dinnington East Riding of Yorkshire S25 3AF, GB

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Medivest Group (Owner Number: 10089556)

Owner / Operator Contact Address

unit 8, Kingfisherway, Dinnington, GB-ERY S25 3AF, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K120833

PMA Number

N/A

All Registered Proprietary Names

OEC 9900 Elite C-Arm Siemens Biograph 64 PET/CT DISCOVERY MR750W 3T Hologic Dimensions 3D mammo Siemens Symbia T16 SPECT/CT Philips Ingenuity 128 CT GE 1.5T EXCITE HDXT MR Siemens YSIO Rad Room GE Discovery 670 SPECT/CT GE Revolution CT Hologic Selenia Dimensions 2D Mammo GE Discovery 750HD CT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OWB	Interventional Fluoroscopic X-Ray System	Radiology	Class 2	892.1650	2024-06-27
OXO	Image-Intensified Fluoroscopic X-Ray System, Mobile	Radiology	Class 2	892.1650	2024-06-27
JAA	System, X-Ray, Fluoroscopic, Image-Intensified	Radiology	Class 2	892.1650	2024-06-27
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2025-05-23
KPS	System, Tomography, Computed, Emission	Radiology	Class 2	892.1200	2025-05-23
LNH	System, Nuclear Magnetic Resonance Imaging	Radiology	Class 2	892.1000	2024-09-04
LNI	System, Nuclear Magnetic Resonance Spectroscopic	Radiology	Class 2	892.1000	2024-09-04
MOS	Coil, Magnetic Resonance, Specialty	Radiology	Class 2	892.1000	2024-09-04
OTE	Digital Breast Tomosynthesis	Unknown	Class 3	N/A	2024-06-27
KPS	System, Tomography, Computed, Emission	Radiology	Class 2	892.1200	2025-04-29
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2025-04-29
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2026-05-22
LNH	System, Nuclear Magnetic Resonance Imaging	Radiology	Class 2	892.1000	2024-04-16
KPR	System, X-Ray, Stationary	Radiology	Class 2	892.1680	2025-02-10
KPS	System, Tomography, Computed, Emission	Radiology	Class 2	892.1200	2025-02-13
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2025-02-13
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2025-04-29
MUE	Full Field Digital, System, X-Ray, Mammographic	Radiology	Class 2	892.1715	2026-03-02
JAK	System, X-Ray, Tomography, Computed	Radiology	Class 2	892.1750	2025-05-23

Official Correspondent

steven dennison

US Agent Details

Mackenzie Dryer Business: Block Imaging Email: mackenzie.dryer@blockimaging.com Phone: (517) 9997099

Related Public Records

Same Entity

Medivest Group

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
K163715	Philips Medical Systems Nederland B.V.	Allura Xper R9	2017-01-26
K060344	Breakaway Imaging, LLC	O-ARM IMAGING SYSTEM	2006-03-29
K982706	Philips Medical Systems, Inc.	PHILIPS BV300 SERIES RELEASE 2.1	1998-09-02
K863853	Superior Medical Products	EAZY COVERS	1987-03-06
K953974	Medivision Medical Imaging, Ltd.	CAMVISION 1000	1996-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2026	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands	2	Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0002-2026	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands	2	Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0003-2026	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands	2	Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0004-2026	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands	2	Allura Xper FD10 OR Table; Model Numbers: 722033; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0005-2026	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands	2	Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

Similar Registrations

Registration Number	Establishment Name	Location
3021027284	ANGIOWAVE IMAGING, INC.	Concord, MA, US
3042175844	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	BEST Noord-Brabant, NL
3027373189	LIBERTY GLOBAL, LLC	Scottsdale, AZ, US
3033527282	Philips India Limited - Image Guided Therapy Systems Business Unit	Bengaluru Karnataka, IN
9614698	CANON INC.	OTAWARA-SHI Tochigi, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027339477. Last updated year: 2026. Please use registration number 3027339477 when referencing this establishment in official correspondence.