PELEGON LLC

FDA Device Registration & Listing · Newark, DE, US · Registration 3029663088

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
3029663088
FEI Number
3029663088
Entity Name
PELEGON LLC
City/State/Country
Newark, DE, US
Establishment Address
200 Continental Drive, Suite 401, Newark, DE 19713, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PELEGON LLC (Owner Number: 10088686)
Owner / Operator Contact Address
200 Continental Drive, Suite 401, Newark, DE 19713, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Adaptor, Hygiene - PELEGON Toilet Safety Rail, PELEGON Raised Toilet Seat

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILS Adaptor, Hygiene Physical Medicine Class 1 890.5050 2023-10-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PELEGON 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
K830425 Maddak, Inc. TOILET SEAT RAISED 1983-05-09

Similar Registrations

Registration Number Establishment Name Location
3010875172 COMMUNITY MEDICAL PRODUCTS LLC Prairie du Sac, WI, US
3043126945 DONGGUAN QIANHE ELECTRONIC TECHNOLOGY CO., LTD. Dongguan Guangdong, CN
3032027168 GUANGDONG ZHONGZE ALUMINUM CO., LTD Foshan Guangdong, CN
3019502344 FOSHAN MAIKANG MEDICAL EQUIPMENT CO., LTD Foshan Guangdong, CN
3004126239 MERCHSOURCE LLC Irvine, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029663088. Last updated year: 2026. Please use registration number 3029663088 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.