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Tsolution One Surgical System

FDA UDI

Class II (US FDA UDI)

by Think Surgical Inc.

Identity

Trade Name
Tsolution One Surgical System FDA UDI
Generic Name
Bone cutter FDA UDI
Device Name
CUTTER 8.25MM FDA UDI
Model / Reference
102862-NS FDA UDI
Description
CUTTER 8.25MM FDA UDI

Identifiers

Primary DI / UDI-DI
M946102862NS0 FDA UDI
510(k) Number
K153647 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Bone cutter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 8.25 Millimeter FDA UDI

Category: Bone cutter

Tsolution One Surgical System by Think Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Think Surgical Inc.

Sources (1)

  • FDA UDI efa5e80a-2018-46e4-88d3-5c33015d0198 36 fields · synced May 30, 2026