← Back to catalogue

Provident Hip System

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
Provident Hip System FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
Lateral Stem FDA UDI
Model / Reference
SC2658-7.5 FDA UDI
Description
Lateral Stem FDA UDI

Identifiers

Primary DI / UDI-DI
10840843107262 FDA UDI
FDA Product Code
LWJ FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

Provident Hip System by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit femoral stem prosthesis.

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

Manufacturer
Globus Medical, Inc.

Sources (1)

  • FDA UDI 50f2fb3f-8a10-41ca-82ec-0b7253dce266 33 fields · synced Jun 1, 2026