DIABETIS JSC

FDA Device Registration & Listing · Vilnius Vilniaus Apskritis, LT · Registration 3022140314

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022140314
FEI Number
3022140314
Entity Name
DIABETIS JSC
City/State/Country
Vilnius Vilniaus Apskritis, LT
Establishment Address
Gedimino ave. 22-41, Vilnius Vilniaus Apskritis LT-01103, LT
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Diabetis JSC (Owner Number: 10083732)
Owner / Operator Contact Address
Gedimino ave. 22-41, Vilnius, LT-VL 01103, LT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Feetsee

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OIZ Foot Examination Tool For Inflammatory Changes Physical Medicine Class 1 890.5050 2022-03-17

Official Correspondent

Rytis Zajanckauskas

US Agent Details

Joseph Teleoglou Email: joe@jtiplaw.com Phone: (714) 3295118

Related Public Records

Same Entity

Diabetis JSC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022140314. Last updated year: 2026. Please use registration number 3022140314 when referencing this establishment in official correspondence.
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