Identity
- Trade Name
- OrthoMedFlex FDA UDI
- Generic Name
- Non-constrained polyethylene acetabular liner FDA UDI
- Device Name
- Tryon (Logical) Liner, +4 Neutral, 36mm Head, Size 52-54mm, X Linked UHMW-PE FDA UDI
- Model / Reference
- 111127652 FDA UDI
- Description
- Tryon (Logical) Liner, +4 Neutral, 36mm Head, Size 52-54mm, X Linked UHMW-PE FDA UDI
Identifiers
- Catalog Number
- 111-12-7652 FDA UDI
- Primary DI / UDI-DI
- M7161111276520 FDA UDI
- FDA Product Code
- LPH FDA UDI
- GMDN Term
- Non-constrained polyethylene acetabular liner 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Non-constrained polyethylene acetabular liner
OrthoMedFlex by Orthomedflex Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Non-constrained polyethylene acetabular liner.
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- PINNACLE — DEPUY ORTHOPAEDICS, INC. · Class II
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
- Orthomedflex Llc
Sources (1)
- FDA UDI 92318785-b4c8-4a87-9e13-e31bcfad838e 34 fields · synced Jun 8, 2026