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Djo Surgical

FDA UDI

Class III (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Revision coated hip femur prosthesis FDA UDI
Device Name
LIMA MODULAR REVISION HIP Revision Body, Std. FDA UDI
Model / Reference
428-00-110 FDA UDI
Description
LIMA MODULAR REVISION HIP Revision Body, Std. FDA UDI

Identifiers

Primary DI / UDI-DI
00888912081306 FDA UDI
510(k) Number
K092331 FDA UDI
FDA Product Code
KWA FDA UDI
KWZ FDA UDI
LZO FDA UDI
LWJ FDA UDI
GMDN Term
Revision coated hip femur prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3330 FDA UDI
888.3310 FDA UDI
888.3353 FDA UDI
888.3360 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: Revision coated hip femur prosthesis

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

Similar devices

Also classified as Revision coated hip femur 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 51ea707a-e40a-4f62-be64-bb6535e7e818 34 fields · synced May 30, 2026