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Cordera Hip System (Stainless Steel) Trial Neck 132degree, 29.0mm

FDA UDI

Class II (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
Cordera Hip System (Stainless Steel) Trial Neck 132degree,29.0mm FDA UDI
Generic Name
Femoral stem prosthesis trial FDA UDI
Device Name
(Stainless Steel) Trial Neck 132degree,29.0mm FDA UDI
Model / Reference
1080-652 FDA UDI
Description
(Stainless Steel) Trial Neck 132degree,29.0mm FDA UDI

Identifiers

Catalog Number
1080-652 FDA UDI
Primary DI / UDI-DI
00810933031152 FDA UDI
510(k) Number
K202484 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Femoral stem prosthesis trial 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Femoral stem prosthesis trial

Cordera Hip System (Stainless Steel) Trial Neck 132degree, 29.0mm by Conformis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral stem prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI 5174395b-b0dd-476e-bdb3-1b9d71167e88 37 fields · synced Jun 8, 2026