DynaMatrix/Dynamatrix Plus
FDA 510(k) K161762 · Cook Biotech Incorporated
510(k) numberK161762
Submission
- Device name
- DynaMatrix/Dynamatrix Plus
- Applicant
- Cook Biotech Incorporated
West Lafayette, IN, US - Received
- June 27, 2016
- Decision date
- January 13, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- NPL – Barrier, Animal Source, Intraoral
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.3930
- Specialty
- Dental
- Implant
- Yes
An animal source dental barrier is an animal-derived material device, such as collagen, intended to aid in guided tissue/bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials when placed around implants.
Other 510(k)s with product code NPL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K242817 | Jason membraneNPL · Traditional | Botiss Biomaterials GmbH | 12/12/2025SE |
| K250512 | Augmented Gingival MatrixNPL · Traditional | Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd. | 12/05/2025SE |
| K252253 | Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®NPL · Traditional | Geistlich Pharma AG | 11/25/2025SE |
| K251062 | Geistlich Bio-Gide; Geistlich Bio-Gide® Shape; Geistlich Bio-Gide® Compressed; Geistlich…NPL · Traditional | Geistlich Pharma AG | 08/14/2025SE |
| K250833 | SwissMembrane X; SwissMembrane X SocketNPL · Special | Geistlich Pharma AG | 04/15/2025SE |
| K233203 | Soft Tissue Augmentation Resorbable MatrixNPL · Traditional | Collagen Matrix, Inc. | 05/01/2024SE |
| K231513 | Oral MatrixNPL · Traditional | Beijing Biosis Healing Biolog Ical Technology… | 02/16/2024SE |
| K231305 | Endoform Dental MembraneNPL · Traditional | Aroa Biosurgery , Ltd. | 01/23/2024SE |
| K230091 | THE CoverNPL · Traditional | Purgo Biologics, Inc. | 10/06/2023SE |
| K223912 | InterCollagen® GuideNPL · Traditional | Sigmagraft, Inc. | 08/17/2023SE |
More from Sigmagraft, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K232646 | Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly…KHJ · Traditional | 05/24/2024SE |
| K201000 | Biodesign Staple Line ReinforcementFTM · Traditional | 07/13/2020SE |
| K191696 | Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix…OXN · Traditional | 12/27/2019SE |
| K171817 | Biodesign Diaphragmatic Hernia GraftFTM · Traditional | 03/13/2018SE |
| K162934 | Biodesign Parastomal Hernia Repair GraftFTM · Traditional | 07/10/2017SE |
| K170016 | Biodesign Fistula PlugFTM · Traditional | 06/21/2017SE |
| K170945 | Biodesign Staple Line ReinforcementOXE · Special | 04/28/2017SE |
| K162741 | AxoGuard Nerve ConnectorJXI · Special | 10/31/2016SE |
| K160136 | Flowable Wound MatrixKGN · Traditional | 09/28/2016SE |
| K161221 | Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula PlugFTM · Special | 05/26/2016SE |
Questions and answers
When was DynaMatrix/Dynamatrix Plus cleared by the FDA?
DynaMatrix/Dynamatrix Plus (K161762) received a 510(k) decision of Substantially Equivalent on January 13, 2017, 200 days after the submission was received.
What is the product code of K161762?
The FDA product code is NPL – Barrier, Animal Source, Intraoral, a Class II (moderate risk) device regulated under 21 CFR 872.3930.