Think Surgical Inc.

FDA Device Registration & Listing · Fremont, CA, US · Registration 3000719653

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3000719653
FEI Number
3000719653
Entity Name
Think Surgical Inc.
City/State/Country
Fremont, CA, US
Establishment Address
47201 Lakeview Blvd, Fremont, CA 94538, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Think Surgical Inc. (Owner Number: 10028805)
Owner / Operator Contact Address
47201 Lakeview Blvd, Fremont, CA 94538, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230202
PMA Number
N/A

All Registered Proprietary Names

TMINI Miniature Robotic System TMINI Miniature Robotic System (TMINI 1.1) TMINI Miniature Robotic System TMINI Miniature Robotic System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-01-08
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2024-09-13
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2024-07-29
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2023-05-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Think Surgical Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3000719653. Last updated year: 2026. Please use registration number 3000719653 when referencing this establishment in official correspondence.
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