Celluheal CS1022
Celluheal CS1022 is a device classified as Unclassified made by Human Biosciences Inc., listed in FDA GUDID since 28 Sep 2023 (UDI-DI 00850048866034), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850048866034 | Date28 Sep 2023 | StatusListed |
Official records
- AccessGUDID record 00850048866034
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Celluheal
- Generic name
- Animal-derived wound matrix dressing
- Model / reference
- CS1022
- Primary DI / UDI-DI
- 00850048866034
- FDA product code
- KGN
- GMDN term
- Animal-derived wound matrix dressing
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KGN (Wound Dressing With Animal-Derived Material(S)).
- MESO WOUND MATRIX by Kensey Nash Corp.
- neoplug by COLLAGEN MATRIX, INC.
- DRESSSKIN by TEI BIOSCIENCES INC.
- ARCHITECT PX EXTRACELLULAR COLLAGEN MATRIX by Harbor Medtech, Inc.
- PriMatrix® 607-004-660 by TEI BIOSCIENCES INC.
- FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATE by Johnson & Johnson Medical, Inc.
- PuraPly Micronized Wound Matrix (PuraPly MZ) by ORGANOGENESIS INC.
- PROCOLL by Innocoll Pharmaceuticals
- epi-ConneKt™ Wound Matrix by Mlm Biologics, Inc.
- MicroMatrix® Flex by ACELL, INC.