Braun Aura 7 (6041)
K-Number: K261975 · 2026-09-30
Device Summary
Frequently Asked Questions
What is the Braun Aura 7 (6041)?
Braun Aura 7 (6041) is a medical device that received FDA 510(k) clearance on 2026-09-30. The listed applicant is CyDen Limited. The 510(k) number is K261975.
When did Braun Aura 7 (6041) receive FDA 510(k) clearance?
Braun Aura 7 (6041) received FDA 510(k) clearance on 2026-09-30, under 510(k) number K261975.
Who is the listed applicant for Braun Aura 7 (6041)?
The FDA 510(k) record lists CyDen Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Braun Aura 7 (6041)?
The FDA product code for Braun Aura 7 (6041) is OHT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing CyDen Limited as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OHT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.