Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004024638

FEI Number

3004024638

Entity Name

LEADING LADY, INC.

City/State/Country

BEACHWOOD, OH, US

Establishment Address

24050 COMMERCE PARK DR., Suite #101, BEACHWOOD, OH 44122, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Golda, Inc. (Owner Number: 9070987)

Owner / Operator Contact Address

24050 COMMERCE PARK DR., --Suite #101, Beachwood, OH 44122, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Surgi-bra, Surgi-vest

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSD	Binder, Abdominal	General Hospital	Class 1	880.5160	2005-06-06
HEF	Binder, Breast	General Hospital	Class 1	880.5160	2005-06-06

Official Correspondent

Donald Burck

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Golda, 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 3004024638. Last updated year: 2026. Please use registration number 3004024638 when referencing this establishment in official correspondence.