Cascade (UDI 910044)
Manufactured by Musculoskeletal Transplant Foundation, Inc.
Device Regulatory Overview
The Cascade (Model/Catalog Number: 910044) is a medical device manufactured by Musculoskeletal Transplant Foundation, Inc.. This product is indexed under FDA Product Code / Category Classification KSS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
QuickGraft Model # 430PST...
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler....
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from ...
Technical Specifications
- Model Number
- 910044
- Product Code / EMDN
- KSS
- Device Name
- Autologous Platelet System Membrane
- Database Sync Date
- 2026-08-09 09:49:20
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Cascade?
The registered manufacturer of record for Cascade is Musculoskeletal Transplant Foundation, Inc..
What is the Primary UDI-DI identifier for Cascade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 910044.
What classification code is assigned to this device?
This device is registered under product classification code KSS.
Similar Classification Devices (KSS)
Other Devices by Musculoskeletal Transplant Foundation, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint