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Djo Surgical

FDA UDI

Class II (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
CLP® HIP SYSTEM Revision Standard Offset Stem FDA UDI
Model / Reference
426-02-100 FDA UDI
Description
CLP® HIP SYSTEM Revision Standard Offset Stem FDA UDI

Identifiers

Primary DI / UDI-DI
00888912079440 FDA UDI
510(k) Number
K052320 FDA UDI
FDA Product Code
KWL FDA UDI
KWA FDA UDI
KWZ FDA UDI
LZO FDA UDI
JDI FDA UDI
LWJ FDA UDI
LPH FDA UDI
KWY FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3330 FDA UDI
888.3310 FDA UDI
888.3353 FDA UDI
888.3350 FDA UDI
888.3358 FDA UDI
888.3390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Press-fit femoral stem prosthesis

Djo Surgical by Encore Medical, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit femoral stem prosthesis.

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 77fab732-cfbf-48fb-8409-8e30409d2b37 34 fields · synced May 30, 2026