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PABLO Lower Extremity

FDA UDI

Class I (US FDA UDI)

by tyromotion GmbH

Identity

Trade Name
PABLO Lower Extremity FDA UDI
Generic Name
Virtual-display rehabilitation system, non-supportive, clinical FDA UDI
Device Name
The PABLO Lower Extremity system is a sensor-based therapy system for gait assessment and movement feedback. FDA UDI
Model / Reference
4 FDA UDI
Description
The PABLO Lower Extremity system is a sensor-based therapy system for gait assessment and movement feedback. FDA UDI

Identifiers

Primary DI / UDI-DI
09120077180106 FDA UDI
FDA Product Code
BXB FDA UDI
GMDN Term
Virtual-display rehabilitation system, non-supportive, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5380 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Virtual-display rehabilitation system, non-supportive, clinical

PABLO Lower Extremity by tyromotion GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Virtual-display rehabilitation system, non-supportive, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
tyromotion GmbH

Sources (1)

  • FDA UDI 6768ade3-1481-4d1b-95f4-7b5aa07ca53e 33 fields · synced Jun 8, 2026