LEAN & JONES, INC.

FDA Device Registration & Listing · Jenkintown, PA, US · Registration 2531819

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
2531819
FEI Number
3002737239
Entity Name
LEAN & JONES, INC.
City/State/Country
Jenkintown, PA, US
Establishment Address
261 Old York Rd Ste 603A, Jenkintown, PA 19046, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
LEAN & JONES, INC. (Owner Number: 9039339)
Owner / Operator Contact Address
261 old york rd #603A, --, Jenkintown, PA 19046, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

dumont

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2026-01-02

Official Correspondent

DAVID DAVIS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LEAN & JONES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2531819. Last updated year: 2026. Please use registration number 2531819 when referencing this establishment in official correspondence.
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