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Trexo Robotics

FDA UDI

Class II (US FDA UDI)

by Trexo Robotics Inc.

Identity

Trade Name
Trexo Robotics FDA UDI
Generic Name
Programmable ambulation exoskeleton, clinical FDA UDI
Device Name
Trexo Robotics XL Trexo Plus 1 Shipment FDA UDI
Model / Reference
A0001 FDA UDI
Description
Trexo Robotics XL Trexo Plus 1 Shipment FDA UDI

Identifiers

Catalog Number
A001BPX FDA UDI
Primary DI / UDI-DI
00628719321072 FDA UDI
FDA Product Code
IKK FDA UDI
GMDN Term
Programmable ambulation exoskeleton, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1925 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Programmable ambulation exoskeleton, clinical

Trexo Robotics by Trexo Robotics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Programmable ambulation exoskeleton, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trexo Robotics Inc.

Sources (1)

  • FDA UDI 18573db6-afaf-42f9-b82d-fdf3dae366ea 35 fields · synced May 30, 2026