Qbtech AB

Stockholm, SE

QBTECH AB appears in FDA device records in Stockholm, SE. FDA records list 4 510(k) clearances between 2004-06-22 and 2016-03-22, no PMA records and 2 registered establishments. As of 2026-09-10, FDA records show no recalls for this company, and at least one establishment registration is current.

510(k) clearances: 4
PMA records: 0
Recall records: 0
Registered establishments: 2

510(k) clearance history

FDA records hold 4 510(k) clearances for Qbtech AB between 2004 and 2016. The busiest year on record is 2004, with 1. The most recent is 2016, with 1.

Clearances by year, as a table

510(k) clearance decisions for Qbtech AB, by decision year
Year	Clearances
2004	1
2012	1
2014	1
2016	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K143468	QbCheck	LQD	Substantially Equivalent	2016-03-22
K133382	QB TEST	LQD	Substantially Equivalent	2014-03-24
K122149	QBTES	LQD	Substantially Equivalent	2012-10-17
K040894	QBTEST	LQD	Substantially Equivalent	2004-06-22

Registered establishments

FDA registered establishments for Qbtech AB, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3004529412	3004529412	QBTECH AB	Cardellgatan 1, Stockholm 11436 SE	2026	LQD
3023138809	3023138809	Qbtech Inc	8 Greenway Plz Ste 750, Houston, TX 77046 US	2026	LQD

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

LQDRecorder, Attention Task Performance

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain