OMNIlife science, Inc.

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3013682146

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
3013682146
FEI Number
3013682146
Entity Name
OMNIlife science, Inc.
City/State/Country
Milpitas, CA, US
Establishment Address
880 N McCarthy Blvd, Suite 220, Milpitas, CA 95035, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Corin Group (Owner Number: 9012268)
Owner / Operator Contact Address
THE CORINIUM CENTRE, --, CIRENCESTER, GB-GLS GL7 1YJ, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K163338
PMA Number
N/A

All Registered Proprietary Names

OMNIBotics Knee System TOTAL KNEE SURGETICS NAVIGATION SYSTEM WITH IBLOCK OMNIBotics Knee System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-12-31
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-12-31
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-12-31

Official Correspondent

Aaron Brunt

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Corin Group
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9614209 Corin Limited CIRENCESTER Gloucestershire, GB
1226188 OMNIlifeScience, Inc. Raynham, MA, US
3012916784 OPTIMIZED ORTHO PTY LTD Sydney New South Wales, AU

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013682146. Last updated year: 2026. Please use registration number 3013682146 when referencing this establishment in official correspondence.
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