Company · DE

Aktormed GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (1 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
NAY	System, Surgical, Computer Controlled Instrument	2
QZB	Software Controlled Endoscope And Instrument Holder	2
OCV	Endoscope Holder	1

Decided	510(k)	Device and applicant	Code
Jul 20, 2026	K261573	ENDOSCOPE HOLDER (182214) Aktormed GmbH, DE	QZB
Aug 8, 2024	K233312	SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip solo voice (202445); SOLOASSIST II (141364) Aktormed GmbH, DE	QZB
Apr 25, 2024	K232405	ENDOFIX EXO Aktormed GmbH, DE	OCV
Dec 22, 2020	K200473	SoloAsisst II, Voice Control Aktormed GmbH, DE	NAY
Sep 21, 2018	K171947	SOLOASSIST II Aktormed GmbH, DE	NAY

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.