FDA.reportPublic FDA data

PERFLEX

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30115327313011532731PERFLEX LTD1N2026-01-014 Hamelacha str. New Ind. Area Netanya Central IL 4250539

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
07290110501990Perflex Biosens - Biosens Thermoplastic pellets for dentures by injection moldingShade Light Dark Mahari1kg net filled in jar and packed in box+97298825473vidal@perflexltd.com
07290110502003Perflex Biosens - Biosens Thermoplastic pellets for dentures by injection moldingShade Light Dark Mahari200gr. net filled in jar and packed in box+97298825473vidal@perflexltd.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1779391528651908K150454Acryfree Denture Base Material and Biosens Denture Base MaterialEBI2015-05-26
1779391376734641
1779391441094774

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EBI12015-05-26

PMN#

GUDID#

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