CIRCINUS MEDICAL TECHNOLOGY, LLC

FDA Device Registration & Listing · Concord, MA, US · Registration 3025394757

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
3025394757
FEI Number
3025394757
Entity Name
CIRCINUS MEDICAL TECHNOLOGY, LLC
City/State/Country
Concord, MA, US
Establishment Address
100-7 Domino Dr., Concord, MA 01742, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Circinus Medical Technology, LLC (Owner Number: 10086779)
Owner / Operator Contact Address
100-7 Domino Dr., Concord, MA 01742, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K213768
PMA Number
N/A

All Registered Proprietary Names

Bolt Navigation System

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 2022-12-11

Official Correspondent

Patrick West

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Circinus Medical Technology, LLC
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

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 3025394757. Last updated year: 2026. Please use registration number 3025394757 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.