Identity
- Trade Name
- Vista Ankle FDA UDI
- Generic Name
- Ankle-disarticulation prosthesis FDA UDI
- Device Name
- a universal single axis prosthetic ankle for elevated vacuum suspension FDA UDI
- Model / Reference
- CA500-BMP FDA UDI
- Description
- a universal single axis prosthetic ankle for elevated vacuum suspension FDA UDI
Identifiers
- Catalog Number
- CA500-BMP FDA UDI
- Primary DI / UDI-DI
- 00850013242283 FDA UDI
- FDA Product Code
- ISY FDA UDI
- GMDN Term
- Ankle-disarticulation prosthesis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ankle-disarticulation prosthesis
Vista Ankle by Cypress Adaptive, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ankle-disarticulation prosthesis.
- Vista Ankle Hydraulic — CYPRESS ADAPTIVE, LLC · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Cypress Adaptive, Llc
Sources (1)
- FDA UDI 76548607-3b66-4e21-a0dc-775e28f8d675 34 fields · synced May 30, 2026