← Back to catalogue

Djo Surgical

FDA UDI

Class II (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Metallic acetabular liner FDA UDI
Device Name
EMPOWR Acetabular, Dual Mobility, Metal Liner, 40E FDA UDI
Model / Reference
951-01-40E FDA UDI
Description
EMPOWR Acetabular, Dual Mobility, Metal Liner, 40E FDA UDI

Identifiers

Primary DI / UDI-DI
00190446668992 FDA UDI
510(k) Number
K203557 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Metallic acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

No

FDA UDI

Category: Metallic acetabular liner

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

Similar devices

Also classified as Metallic acetabular liner.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b5136f19-cd90-4bad-a8c1-3624a5f82f33 34 fields · synced May 31, 2026