Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Collagen Matrix with 47 510(k) clearances and 15 device recalls. The most recent is a 510(k) clearance dated Nov 18, 2025: Collagen Dura Regeneration Membrane - Repair.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 18, 2025 | Collagen Dura Regeneration Membrane - RepairK251191 · GXQ | 510(k) clearances |
| Dec 19, 2024 | Bovine Dermis Collagen Dermal MatrixK243071 · KGN | 510(k) clearances |
| Oct 2, 2024 | RejuvaKnee™ Collagen Meniscus ImplantK242302 · OLC | 510(k) clearances |
| May 1, 2024 | Soft Tissue Augmentation Resorbable MatrixK233203 · NPL | 510(k) clearances |
| Mar 12, 2024 | Mineral Collagen Composite Bioactive Moldable Bone Graft MatrixK240424 · MQV | 510(k) clearances |
| Aug 2, 2023 | Mineral Collagen Composite Bioactive Extra MoldableK231942 · MQV | 510(k) clearances |
| Dec 20, 2022 | Mineral Collagen Composite Bioactive MoldableK221735 · MQV | 510(k) clearances |
| May 31, 2022 | Fibrillar Collagen Wound DressingK213341 · KGN | 510(k) clearances |
| Dec 13, 2021 | DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45Class II · Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, wh | Device recalls |
| Dec 13, 2021 | RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matter. REF: DUMO10125Class II · Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, wh | Device recalls |
| Mar 19, 2019 | Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable Class II · Product was packaged in the wrong box; may have been placed inside a Neomem FLEXPLUS box instead of a Neomem box | Device recalls |
| Aug 16, 2018 | BioMend Extend, REF# 0142Z, Synthetic bone grafting material.Class III · There is a possibility that the product was packaged in the wrong box. Specifically, the product may have been placed i | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
