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XACT ACE Xtend

FDA UDI

Class II (US FDA UDI)

by Xact Robotics Ltd

Identity

Trade Name
XACT ACE Xtend FDA UDI
Generic Name
Computer/medical device keyboard FDA UDI
Device Name
XACT ACE Xtend FDA UDI
Model / Reference
B FDA UDI
Description
XACT ACE Xtend FDA UDI

Identifiers

Catalog Number
XR-ACE-XTEND FDA UDI
Primary DI / UDI-DI
07290017702384 FDA UDI
510(k) Number
K221116 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Computer/medical device keyboard FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Computer/medical device keyboard

XACT ACE Xtend by Xact Robotics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Computer/medical device keyboard.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xact Robotics Ltd

Sources (1)

  • FDA UDI 65d0a382-cda2-4d31-93f7-74915f6ef3fe 36 fields · synced Jun 1, 2026