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Medical Positioning, Inc.

US

Last updated September 17, 2026

About

MedicalPositioning offers unique, ergonomic, innovative, and proven products that position you for the best possible results.

From the manufacturer's own website. Source

Information

Country
US
Address
9738 Pflumm Road, Lenexa, KS, 66215
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1000118382
DUNS Number
—

Catalogue (59)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
EchoTable 073
FDA UDI
Class IActive
UltraScan Versa Premier 292
FDA UDI
Class IActive
VizaVue 5500
FDA UDI
Class IActive
Stress Echo Bed 1730
FDA UDI
Class IActive
EchoTable 572-C
FDA UDI
Class IActive
HUT Table 1211
FDA UDI
Class IActive
HUT Table 1031
FDA UDI
Class IActive
UltraMamm 952
FDA UDI
Class IActive
RR HUT Table 1058
FDA UDI
Class IActive
EchoTable 272
FDA UDI
Class IActive
UltraScan Versa 087-C
FDA UDI
Class IActive
VasScan Table X 084
FDA UDI
Class IActive
Ergometer 1505
FDA UDI
Class IActive
EchoOne 4152
FDA UDI
Class IActive
RR HUT Table 1056
FDA UDI
Class IActive
EchoTable 072
FDA UDI
Class IActive
VasScan Table X 284
FDA UDI
Class IActive
UltraMamm 052-T
FDA UDI
Class IActive
EchoBed X 222
FDA UDI
Class IActive
UltraScan Versa 995
FDA UDI
Class IActive
EchoBed X 223
FDA UDI
Class IActive
Stress Echo Bed 1736
FDA UDI
Class IActive
UltraScan Versa 287
FDA UDI
Class IActive
UltraScan Versa 295
FDA UDI
Class IActive
RR HUT Table 1258
FDA UDI
Class IActive
GSPM Table 60012
FDA UDI
Class IActive
UltraScan Versa 087
FDA UDI
Class IActive
UltraMamm 052
FDA UDI
Class IActive
Ultra DBI Table 9400
FDA UDI
Class IActive
EchoTable 283
FDA UDI
Class IActive
EchoBed X 233
FDA UDI
Class IActive
EchoOne 4052
FDA UDI
Class IActive
EchoOne 4252
FDA UDI
Class IActive
HUT Table 1231
FDA UDI
Class IActive
EchoTable 273
FDA UDI
Class IActive
EchoBed X 022
FDA UDI
Class IActive
UltraScan Versa 095
FDA UDI
Class IActive
UltraScan Versa 987
FDA UDI
Class IActive
EchoBed X 201
FDA UDI
Class IActive
Ergometer 1505
FDA UDI
Class IActive
HUT Table 1011
FDA UDI
Class IActive
EchoTable 083
FDA UDI
Class IActive
DBI Table 7407
FDA UDI
Class IActive
UltraMamm 452
FDA UDI
Class IActive
RR HUT Table 1256
FDA UDI
Class IActive
UltraScan Versa Premier 992
FDA UDI
Class IActive
GSPM Table 60232
FDA UDI
Class IActive
EchoTable 051
FDA UDI
Class IActive
MultiView 5562
FDA UDI
Class IActive
VasScan X Table 984
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (9)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jul 10, 2014Z-2209-2014—terminated

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Jul 10, 2014Z-2210-2014—terminated

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Jul 10, 2014Z-2208-2014—terminated

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Jul 10, 2014Z-2211-2014—terminated

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Mar 5, 2012Z-1211-2012—terminated

The warning label regarding electrical shock was not placed on the device warning to have the power switch in the "OFF" position prior to connecting the unit to electric power.

Mar 5, 2012Z-1210-2012—terminated

The warning label regarding electrical shock was not placed on the device warning to have the power switch in the "OFF" position prior to connecting the unit to electric power.

Feb 1, 2010Z-1973-2011—terminated

The tilt tables work intermittently and some have become stuck in an inclined or reclined position during procedures.

Feb 1, 2010Z-1975-2011—terminated

The tilt tables work intermittently and some have become stuck in an inclined or reclined position during procedures.

Feb 1, 2010Z-1974-2011—terminated

The tilt tables work intermittently and some have become stuck in an inclined or reclined position during procedures.