Identity
- Trade Name
- DJO SURGICAL FDA UDI
- Generic Name
- Constrained polyethylene acetabular liner FDA UDI
- Device Name
- LINER, ACETABULAR, FMP CONSTRAINED 28XMP10 FDA UDI
- Model / Reference
- 436-28-010 FDA UDI
- Description
- LINER, ACETABULAR, FMP CONSTRAINED 28XMP10 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888912085755 FDA UDI
- 510(k) Number
- K023794 FDA UDI
- FDA Product Code
- KWZ FDA UDI
- GMDN Term
- Constrained polyethylene acetabular liner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3310 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
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: Constrained polyethylene acetabular liner
Djo Surgical by Encore Medical, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Constrained polyethylene acetabular liner.
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- System 12 — Howmedica Osteonics Corp. · Class II
- Trabecular Metal® Acetabular Revision System — Zimmer, Inc. · Class II
- Omnifit — Howmedica Osteonics Corp. · Class II
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- System 12 — Howmedica Osteonics Corp. · Class II
Cleared under the same submission
K023794 also covers:
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — DJO, LLC
- DJO SURGICAL — ENCORE MEDICAL, L.P.
- DJO SURGICAL — ENCORE MEDICAL, L.P.
- DJO SURGICAL — ENCORE MEDICAL, L.P.
- DJO SURGICAL — ENCORE MEDICAL, L.P.
- DJO SURGICAL — ENCORE MEDICAL, L.P.
- DJO SURGICAL — ENCORE MEDICAL, L.P.
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 |
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Manufacturer
- Manufacturer
- Encore Medical, L.p.
Sources (1)
- FDA UDI f6811934-64ab-437d-ae30-9f0a287e03df 34 fields · synced Jun 8, 2026