FDA.reportPublic FDA data

ZYRIS, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
20325743003706371ZYRIS, INC.1N2026-01-016868A Cortona Dr Santa Barbara CA US 93117

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
00810032660765Isolite, i3 - Control Head Hose, i3+1(800)560-6066regulatory@zyris.com
00810032660772Isolite, i3 - Power Vacuum Base, i3+1(800)560-6066regulatory@zyris.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
604041795088643K242435Dental Barrier and SleevesPEM2024-10-18
604041261582833
604041276010125
604041446193238
604041594023928
604041765104379

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PEM12024-10-18

GUDID#

139 records. Showing 1-40. Next