FDA.reportPublic FDA data

ENCORE, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
15279821527982ENCORE, INC.1N2026-01-016487 Parkland Drive Ste 111 SARASOTA FL US 34243

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850358007004Impoaid - VTU-1800-475-3091info@revivepremium.com
00850358007011Encore - Manual Vacuum Erection Device800-475-3091info@revivepremium.com
00850358007400Encore - 44017-RETNP- Vacuum Erection Device - 3 kits800-475-3091info@revivepremium.com
00850358007417Encore - 44017-UNB- Vacuum Erection Device - 3 kits800-475-3091info@revivepremium.com
00850358007424Encore - 44017-UNM- Vacuum Erection Device - 3 kits800-475-3091info@revivepremium.com
10850358007407Encore - 44017-RETNP- Vacuum Erection Device - Master Carton 12800-475-3091info@revivepremium.com
10850358007414Encore - 44017-UNB- Vacuum Erection Device - Master Carton 12800-475-3091info@revivepremium.com
10850358007421Encore - 44017-UNM- Vacuum Erection Device - Master Carton 12800-475-3091info@revivepremium.com

Registered Device Listings#

Registration key, Listing key table
Registration keyListing key
442061838770665

PMN#

GUDID#

45 records. Showing 1-40. Next