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FDA 510(k)

TMINI Miniature Robotic System

K-Number: K261024 · 2026-07-24

Decision Date2026-07-24
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TMINI Miniature Robotic System is the device name listed in this FDA 510(k) record. The listed applicant is THINK Surgical, Inc.. It received FDA 510(k) clearance on 2026-07-24 under 510(k) number K261024. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMINI Miniature Robotic System?

TMINI Miniature Robotic System is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is THINK Surgical, Inc.. The 510(k) number is K261024.

When did TMINI Miniature Robotic System receive FDA 510(k) clearance?

TMINI Miniature Robotic System received FDA 510(k) clearance on 2026-07-24, under 510(k) number K261024.

Who is the listed applicant for TMINI Miniature Robotic System?

The FDA 510(k) record lists THINK Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TMINI Miniature Robotic System?

The FDA product code for TMINI Miniature Robotic System is OLO.

Other records listing THINK Surgical, Inc. 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.

View all 22 devices →

Related Devices (Code: OLO)

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.