Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)
K-Number: K260322 · 2026-06-11
Device Summary
Frequently Asked Questions
What is the Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)?
Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) is a medical device that received FDA 510(k) clearance on 2026-06-11. The listed applicant is Mighty Oak Medical. The 510(k) number is K260322.
When did Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) receive FDA 510(k) clearance?
Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) received FDA 510(k) clearance on 2026-06-11, under 510(k) number K260322.
Who is the listed applicant for Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)?
The FDA 510(k) record lists Mighty Oak Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)?
The FDA product code for Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) is QIH.
Other records listing Mighty Oak Medical 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: QIH)
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.