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Progeny Hip System

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
Progeny Hip System FDA UDI
Generic Name
Uncoated femoral stem prosthesis, one-piece FDA UDI
Model / Reference
SC2069-4 FDA UDI

Identifiers

Primary DI / UDI-DI
10840843103813 FDA UDI
FDA Product Code
JDG FDA UDI
GMDN Term
Uncoated femoral stem prosthesis, one-piece 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: Uncoated femoral stem prosthesis, one-piece

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

Similar devices

Also classified as Uncoated femoral stem prosthesis, one-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c5c11eb-51d0-45a4-8cfb-7af98a88508c 32 fields · synced May 29, 2026