FDA Device Intelligence
HomeBRIGHTWAKE LIMITED › Silflex

Silflex

BRIGHTWAKE LIMITED · Model CR3924 · UDI-DI 05060031472981

NAD
10
510(k) clearances
15,775
Adverse events (7 deaths)
19
Recalls
511
Facilities

Description

Soft silicone wound contact layer 12 cm X 15 cm. A wound contact layer made from polyester mesh and coated with Silfix soft silicone. Silflex is designed to gently adhere to the skin surrounding a wound and not to the wound bed. This is an atraumatic dressing designed to minimise the pain and trauma associated with dressing change. The dressing’s large perforations allow for the passage of exudate and irrigation of wound.

Recalls

DateFirmReason
2025-08-29ConvaTec, IncWound dressing may have foreign matter on the product.
2025-02-19MEDLINE INDUSTRIES, LP - NorthfieldThere is a potential for the sterility of the device to be compromised.
2022-01-28Sam Medical ProductsDue to partially assembled valved dressing that has a hole within it instead of the intended non-valved dressing in the package resulting in that the dressing cannot be centered ov
2021-08-20ConvaTec, IncPrimary packaging labeling may be incorrect.
2021-08-09ConvaTec, IncThere is a potential for open seals which can compromise sterility.
2018-08-01COVIDIEN LLCPotential for product sterility breach due to a compromised or pinched seal defect
2018-08-01COVIDIEN LLCPotential for product sterility breach due to a compromised or pinched seal defect
2018-08-01COVIDIEN LLCPotential for product sterility breach due to a compromised or pinched seal defect
2018-08-01COVIDIEN LLCPotential for product sterility breach due to a compromised or pinched seal defect
2018-08-01COVIDIEN LLCPotential for product sterility breach due to a compromised or pinched seal defect

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.