Identity
- Trade Name
- Revision Femoral Head FDA UDI
- Generic Name
- Ceramic femoral head prosthesis FDA UDI
- Device Name
- Revision Femoral Head - Dia.40 mm M Taper 12/14 FDA UDI
- Model / Reference
- 5010.42.052 FDA UDI
- Description
- Revision Femoral Head - Dia.40 mm M Taper 12/14 FDA UDI
Identifiers
- Catalog Number
- 5010.42.052 FDA UDI
- Primary DI / UDI-DI
- 08033390183666 FDA UDI
- 510(k) Number
- K243809 FDA UDI
- FDA Product Code
- LZO FDA UDILPH FDA UDI
- GMDN Term
- Ceramic femoral head prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 FDA UDI888.3358 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: Ceramic femoral head prosthesis
Revision Femoral Head by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ceramic femoral head prosthesis.
- Ceramic ball head — Beijing LiDaKang Technology Co., Ltd. · Class III
- ELEC(R)plus — HiPer Medical AG · Class III
- BIOLOX® delta Modular Ceramic Head — Biomet Uk Ltd · Class II
- InSitu Hip System — Nextstep Arthropedix · Class II
- Prosthesis Head A — WALDEMAR LINK GmbH & Co. KG · Class II
- InSitu Hip System — Nextstep Arthropedix · Class II
- SYNERGY — Smith & Nephew, Inc. · Class II
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
Cleared under the same submission
K243809 also covers:
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
- Revision Femoral Head — Limacorporate
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Limacorporate
Sources (1)
- FDA UDI e2cc24e4-0537-48fe-b258-6f73f12297b5 36 fields · synced Jun 1, 2026