GIDDY HOLDINGS, INC.

FDA Device Registration & Listing · Austin, TX, US · Registration 3016028125

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
3016028125
FEI Number
3016028125
Entity Name
GIDDY HOLDINGS, INC.
City/State/Country
Austin, TX, US
Establishment Address
1005 E. St. Elmo Road, Bldg. 10, Austin, TX 78745, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Giddy Holdings, Inc. (Owner Number: 10062062)
Owner / Operator Contact Address
1005 E. St. Elmo Road, Bldg. 10, Austin, TX 78745, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Eddie; Giddy Eddie Eddie by Giddy

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LKY Device, External Penile Rigidity Gastroenterology, Urology Class 2 876.5020 2019-12-14

Official Correspondent

Brett Jacobson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Giddy Holdings, 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 3016028125. Last updated year: 2026. Please use registration number 3016028125 when referencing this establishment in official correspondence.
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