FDA.reportPublic FDA data

INSTYLLA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30172086423017208642INSTYLLA, INC.1N2026-01-01201 Burlington Rd, North Building Bedford MA US 01730

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
00812013030055Instylla Microcatheter - N/A781-790-4860xx@xx.xx

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2792332006859213P250003Embrace(TM) Hydrogel Embolic SystemQVG2025-08-05
2792331142122005K253769Instylla Delivery KitFMF2025-12-22
2792331275827878K213632Instylla Delivery KitFMF2022-02-10
2792331237752890K210808Instylla Microcatheter 1.2KRA2021-04-15
2792331990929665K200744Instylla MicrocatheterKRA2020-04-21
2792331087257177K191659Instylla Delivery KitFMF2019-10-10

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FMF32025-12-22
KRA22021-04-15

PMN#

GUDID#