SENECA DEVICES INC

FDA Device Registration & Listing · Durham, NC, US · Registration 3018115441

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
3018115441
FEI Number
3018115441
Entity Name
SENECA DEVICES INC
City/State/Country
Durham, NC, US
Establishment Address
2 Davis Drive #117, Durham, NC 27709, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Seneca Devices Inc (Owner Number: 10080842)
Owner / Operator Contact Address
2 Davis Drive #19, Research Triangle Park, Durham, NC 27709, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EasyShift EasyShift EasyShift SPU Zipper Sheet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKZ Bed, Patient Rotation, Powered Physical Medicine Class 2 890.5225 2022-11-10
FNK Bed, Hydraulic, Adjustable Hospital General Hospital Class 1 880.5110 2022-11-10
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2023-12-22

Official Correspondent

Samuel Fox

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Seneca Devices Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018115441. Last updated year: 2026. Please use registration number 3018115441 when referencing this establishment in official correspondence.
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