← 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
Coated hip femur prosthesis, modular FDA UDI
Device Name
REVELATION HIP STEM 10.5 RT POROUS COATED W/P2 FDA UDI
Model / Reference
427-04-105 FDA UDI
Description
REVELATION HIP STEM 10.5 RT POROUS COATED W/P2 FDA UDI

Identifiers

Primary DI / UDI-DI
00888912080156 FDA UDI
510(k) Number
K973685 FDA UDI
FDA Product Code
LPH FDA UDI
KWZ FDA UDI
KWA FDA UDI
LZO FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coated hip femur prosthesis, modular

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

Similar devices

Also classified as Coated hip femur prosthesis, modular.

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 1321f2f9-4839-48ba-a7e6-003896ca26fd 34 fields · synced Jun 1, 2026