Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032857006

FEI Number

3032857006

Entity Name

PS DEVICES, LLC

City/State/Country

Lyndhurst, OH, US

Establishment Address

29001 Cedar Rd Ste 431, Lyndhurst, OH 44124, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

PS Devices, LLC (Owner Number: 10091515)

Owner / Operator Contact Address

29001 Cedar Rd., Suite 431, Lyndhurst, OH 44124, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bstent intranasal stent

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LYA	Splint, Intranasal Septal	Ear, Nose, Throat	Class 1	874.4780	2024-10-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PS Devices, LLC

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 3032857006. Last updated year: 2026. Please use registration number 3032857006 when referencing this establishment in official correspondence.