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Leander

FDA UDI

Class I (US FDA UDI)

by Leander, Llc

Identity

Trade Name
Leander FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
Examination/treatment motorized table with some articulated sections that can be adjusted into various accommodations for patient comfort and/or treatment. It is typically used by physical therapists and chiropractors. FDA UDI
Model / Reference
L950 FDA UDI
Description
Examination/treatment motorized table with some articulated sections that can be adjusted into various accommodations for patient comfort and/or treatment. It is typically used by physical therapists and chiropractors. FDA UDI

Identifiers

Primary DI / UDI-DI
G509SERIES9000 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
Examination/treatment table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Examination/treatment table, line-powered

Leander by Leander, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/treatment table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Leander, Llc

Sources (1)

  • FDA UDI bf9c67e4-9ada-4042-a813-e7da96eba8d3 33 fields · synced May 31, 2026