ONOCOR LLC

FDA Device Registration & Listing · West Chester, PA, US · Registration 3023548693

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
3023548693
FEI Number
3023548693
Entity Name
ONOCOR LLC
City/State/Country
West Chester, PA, US
Establishment Address
1570 Pocopson Rd, West Chester, PA 19382, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Onocor LLC (Owner Number: 10085947)
Owner / Operator Contact Address
1570 Pocopson Rd, West Chester, PA 19382, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K212988
PMA Number
N/A

All Registered Proprietary Names

ONO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMX Device, Percutaneous Retrieval Cardiovascular Class 2 870.5150 2022-09-16

Official Correspondent

Tiffini Wittwer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Onocor 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
K213494 ABBOTT MEDICAL Aveir Retrieval Catheter 2022-04-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023548693. Last updated year: 2026. Please use registration number 3023548693 when referencing this establishment in official correspondence.
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