Identity
- Trade Name
- Equinoxe FDA UDI
- Generic Name
- Polyethylene reverse shoulder prosthesis cup FDA UDI
- Model / Reference
- 320-36-03 FDA UDI
Identifiers
- Catalog Number
- 320-36-03 FDA UDI
- Primary DI / UDI-DI
- 10885862086624 FDA UDI
- 510(k) Number
- K093275 FDA UDI
- FDA Product Code
- KWS FDA UDIKWT FDA UDI
- GMDN Term
- Polyethylene reverse shoulder prosthesis cup FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 FDA UDI888.3650 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 36 Millimeter FDA UDI
Category: Polyethylene reverse shoulder prosthesis cup
Equinoxe by Exactech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polyethylene reverse shoulder prosthesis cup.
- PERFORM™ HUMERAL SYSTEM — TORNIER, INC. · Class II
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- PERFORM™ HUMERAL SYSTEM — TORNIER, INC. · Class II
- HUMERIS 135 — FX SOLUTIONS · Class II
Cleared under the same submission
K093275 also covers:
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
- Exactech, Inc.
Sources (1)
- FDA UDI 78a0713d-d850-4fe1-ad90-ff56f8200c0a 35 fields · synced Jun 8, 2026