ENCORE, INC.

FDA Device Registration & Listing · SARASOTA, FL, US · Registration 1527982

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
1527982
FEI Number
1527982
Entity Name
ENCORE, INC.
City/State/Country
SARASOTA, FL, US
Establishment Address
6487 Parkland Drive, Ste 111, SARASOTA, FL 34243, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ENCORE MEDICAL, INC. (Owner Number: 9003350)
Owner / Operator Contact Address
6487 Parkland Drive, Ste 111, --, Sarasota, FL 34243, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Revive ImpoAid

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 1992-07-13

Official Correspondent

JACK BENNETT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ENCORE MEDICAL, INC.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1527982. Last updated year: 2026. Please use registration number 1527982 when referencing this establishment in official correspondence.
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