Get started with Re5 in your clinic
  • Evidence review & live demonstration: We walk you through the clinical data and show you the device in action

  • Patient monitoring software: Track treatment progress and compliance (retrospectively)

  • Clinical implementation guidance: Practical help integrating Re5 into your existing treatment pathways

Interested in research collaboration?
  • Investigator-initiated study support: Device supply, technical setup, and regulatory documentation for independent clinical research

  • Access to existing clinical data: Published studies and summary of Clinical Evaluation Report available on request

Peer-reviewed clinical evidence

Backed by science

6+

Peer-reviewed clinical publications - including sham-controlled RCTs, dose-response studies, independent multicenter trials, and real-world outcomes data

34% / 61%

Sham-controlled remission / response in strictly defined TRD (≥2 failed antidepressant courses) in a 5-week treatment protocol, n=50 (Martiny 2010)

~70%

Remission in an 8-week treatment protocol in a dose-response RCT in TRD, n=58 (Straasø 2014)

Zero

Serious Adverse Events in 20,000+ sessions (CER)

29%

Remission in patients who did not respond to ECT, n=19

(Larsen 2020)

100%

Remission in relapsed remitters at 2-year follow-up, n=13 (Bech 2015)

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.