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TELAMax

TELA BIO, INC. · Model F10068-0408 · UDI-DI 10856072005132

FTM Prescription
10
510(k) clearances
11,594
Adverse events (47 deaths)
76
Recalls
89
Facilities

Description

TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. TELAMax will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements.

Recalls

DateFirmReason
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.