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Continuum® Trilogy® Allofit® Vivacit-E®
FDA UDIClass II (US FDA UDI)
by Zimmer, Inc.
Identity
- Trade Name
- Continuum® Trilogy® Allofit® Vivacit-E® FDA UDI
- Generic Name
- Non-constrained polyethylene acetabular liner FDA UDI
- Model / Reference
- 00-8852-006-28 FDA UDI
Identifiers
- Catalog Number
- 00-8852-006-28 FDA UDI
- Primary DI / UDI-DI
- 00889024155442 FDA UDI
- 510(k) Number
- K120370 FDA UDI
- FDA Product Code
- OQI FDA UDIJDI FDA UDIOQH FDA UDILZO FDA UDILPH FDA UDIOQG FDA UDI
- GMDN Term
- Non-constrained polyethylene acetabular liner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 FDA UDI888.3350 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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 28 Millimeter FDA UDI
Category: Non-constrained polyethylene acetabular liner
Continuum® Trilogy® Allofit® Vivacit-E® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Non-constrained polyethylene acetabular liner.
- C-Fit & DC-Fit Acetabular Cup System — CORIN LTD · Class II
- RINGLOC HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- MobileLink Acetabular Cup System — WALDEMAR LINK GmbH & Co. KG · Class II
- PRIME — MicroPort Orthopedics Inc. · Class II
- G7 Acetabular Liner — Biomet Orthopedics, Inc. · Class II
- Logical 20° Hooded Liner — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
- RINGLOC RX90-2 HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- PINNACLE — DEPUY ORTHOPAEDICS, INC. · Class II
Cleared under the same submission
K120370 also covers:
- Continuum® Trilogy® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
- Continuum® Trilogy® Allofit® — Zimmer, Inc.
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
- Zimmer, Inc.
Sources (1)
- FDA UDI 75ef54c8-f33f-452a-98d0-5c3e91b9f53f 36 fields · synced Jun 1, 2026