FDA.reportPublic FDA data

Proprio

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30203755733020375573Proprio1N2026-01-01111 W John St STE 308 Seattle WA US 98119

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
00850042604052Paradigm - Paradigm Blunt Probe2068486303customerservice@propriovision.com
00850042604069Paradigm - Paradigm Straight Pedicle Probe2068486303customerservice@propriovision.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3169531992817250K252950Paradigm SystemOLO2025-12-15
3169531617756562K250879Paradigm SystemOLO2025-06-04
3169531987368568K243258Paradigm SystemOLO2025-02-21
3169531383853507K222291Paradigm SystemOLO2023-04-21

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OLO42025-12-15

PMN#

GUDID#