GID BIO INC.

FDA Device Registration & Listing · Louisville, CO, US · Registration 3009964461

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
3009964461
FEI Number
3009964461
Entity Name
GID BIO INC.
City/State/Country
Louisville, CO, US
Establishment Address
901 Front St Suite 240, Louisville, CO 80027, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
GID BIO INC. (Owner Number: 10042421)
Owner / Operator Contact Address
901 Front Street, Suite 240, Louisville, CO 80027, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SVF-2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTN Plastic Surgery And Accessories Kit General, Plastic Surgery Class 1 878.3925 2016-04-12

Official Correspondent

William Cimino

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GID BIO 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 3009964461. Last updated year: 2026. Please use registration number 3009964461 when referencing this establishment in official correspondence.
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