Identity
- Trade Name
- Invengenx FDA UDI
- Generic Name
- Cardiovascular patch, animal-derived FDA UDI
- Model / Reference
- XM-17 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850038226176 FDA UDI
- 510(k) Number
- K182493 FDA UDI
- FDA Product Code
- FTM FDA UDI
- GMDN Term
- Cardiovascular patch, animal-derived FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 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
- Height — 5 Centimeter FDA UDILength — 6 Centimeter FDA UDI
Category: Cardiovascular patch, animal-derived
Invengenx by Tisgenx — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiovascular patch, animal-derived.
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- VASCU-GUARD Peripheral Vascular Patch — SYNOVIS LIFE TECHNOLOGIES, INC. · Class II
- VascuCel — ADMEDUS REGEN PTY LTD · Class II
- AlboSure Vascular Patch — LeMaitre Vascular, Inc. · Class II
- XenoSure Biologic Patch — LeMaitre Vascular, Inc. · Class II
- AlboSure Vascular Patch — LeMaitre Vascular, Inc. · Class II
Cleared under the same submission
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
- Tisgenx
Sources (1)
- FDA UDI 6184da0d-c2f6-44d1-af9e-4dc62ec1494a 35 fields · synced May 30, 2026