Digital C-ARM with 3D
K-Number: K253296 · 2026-06-05
Device Summary
Frequently Asked Questions
What is the Digital C-ARM with 3D?
Digital C-ARM with 3D is a medical device that received FDA 510(k) clearance on 2026-06-05. The listed applicant is Allengers Medical Systems Limited. The 510(k) number is K253296.
When did Digital C-ARM with 3D receive FDA 510(k) clearance?
Digital C-ARM with 3D received FDA 510(k) clearance on 2026-06-05, under 510(k) number K253296.
Who is the listed applicant for Digital C-ARM with 3D?
The FDA 510(k) record lists Allengers Medical Systems Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Digital C-ARM with 3D?
The FDA product code for Digital C-ARM with 3D is OXO.
Other records listing Allengers Medical Systems 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: OXO)
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.