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KYPHON® Express™ Inflatable Bone Tamp

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
KYPHON® Express™ Inflatable Bone Tamp FDA UDI
Generic Name
Inflatable bone tamp FDA UDI
Device Name
BONE TAMP KE102 10/2 EXPRESS II IBT FDA UDI
Model / Reference
KE102 FDA UDI
Description
BONE TAMP KE102 10/2 EXPRESS II IBT FDA UDI

Identifiers

Primary DI / UDI-DI
00643169143791 FDA UDI
510(k) Number
K123771 FDA UDI
FDA Product Code
HXG FDA UDI
HRX FDA UDI
GMDN Term
Inflatable bone tamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inflatable bone tamp

KYPHON® Express™ Inflatable Bone Tamp by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inflatable bone tamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 947447bf-ddba-44f6-884a-e6871ad149b6 35 fields · synced Jun 1, 2026