510(k) Report

FDA applicant

Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S

Istanbul, TR1 decision2015–20150 recalls

FDA records 1 decision for Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S (Istanbul, TR) in 2015: 1 510(k) clearance. All are in product code IPL (Wheelchair, Standup). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Matia”

FDA records each applicant name separately; these may or may not be the same firm.