Identity
- Trade Name
- REFLECTION FDA UDI
- Generic Name
- Polyethylene acetabulum prosthesis FDA UDI
- Device Name
- REFLECTION ALL POLY ACETABULAR COMP 28MM INNER DIAMETER 55MM OUTER DIAMETER 20 DEGREE XLPE FDA UDI
- Model / Reference
- 71358026 FDA UDI
- Description
- REFLECTION ALL POLY ACETABULAR COMP 28MM INNER DIAMETER 55MM OUTER DIAMETER 20 DEGREE XLPE FDA UDI
Identifiers
- Catalog Number
- 71358026 FDA UDI
- Primary DI / UDI-DI
- 03596010481818 FDA UDI
- 510(k) Number
- K002747 FDA UDI
- FDA Product Code
- JDI FDA UDI
- GMDN Term
- Polyethylene acetabulum prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3350 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: Polyethylene acetabulum prosthesis
Reflection by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Polyethylene acetabulum prosthesis.
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- Exeter — Howmedica Osteonics Corp. · Class II
- Exeter — Howmedica Osteonics Corp. · Class II
- ZCA® — Zimmer, Inc. · Class II
- ZCA® — Zimmer, Inc. · Class II
- ONVOY — GLOBUS MEDICAL, INC. · Class II
Cleared under the same submission
K002747 also covers:
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, Inc.
- REFLECTION — Smith & Nephew, 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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 3572edc7-95b8-4fb8-9083-391b80c0c1a7 36 fields · synced Jun 8, 2026