Atlas FDA

SiOxD Wound Matrix

FDA 510(k) clearance K232847 · decided 2023-12-18

Clearance details

K-number
K232847
Device name
SiOxD Wound Matrix
Applicant
Sioxmed, LLC
Decision
Substantially Equivalent
Date received
2023-09-14
Decision date
2023-12-18
Days to decision
95 days
Clearance type
Traditional
Product code
QSZ
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Clemmons, NC, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Redermo Wound Matrix (K260020)Beijing Kreate Medical Co., Ltd.2026-04-16
NovoSorb BTM (K251567)Polynovo Biomaterials Pty, Ltd.2025-06-20
NovoSorb® MTX (K242149)Polynovo Biomaterials Pty, Ltd.2025-03-05
SiOxD® Wound Matrix (K241660)Sioxmed, LLC2024-07-05
Restrata® MiniMatrix (K223725)Acera Surgical, Inc.2023-05-18
SiOxD Wound Matrix (K222189)Sioxmed, LLC2022-11-18
NovoSorb Matrix (K221686)Polynovo Biomaterials Pty, Ltd.2022-09-15
Restrata® (K193583)Acera Surgical, Inc.2020-09-25
Phoenix Wound Matrix (K173544)Nanofiber Solutions, Inc.2018-03-02
NovoSorb BTM Wound Dressing (2cm x 2cm), NovoSorb BTM Wound Dressing (10cm x 10cm), NovoSorb BTM Wound Dressing (10cm x 20cm), NovoSorb BTM Wound Dressing (20cm x 40cm) (K172140)Polynovo Biomaterials Pty, Ltd.2017-08-11
SupraSDRM Biodegradable Matrix Wound Dressing (K170213)Polymedics Innovations, GmbH2017-06-28
Restrata Wound Matrix (K170300)Acera Surgical, Inc.2017-04-26

Recalls involving this device

No recalls on record reference this clearance.