Restrata

K261245 · Acera Surgical, Inc. · QSZ · Oct 16, 2026 · SU

Device Facts

Record IDK261245
Device NameRestrata
ApplicantAcera Surgical, Inc.
Product CodeQSZ · SU
Decision DateOct 16, 2026
DecisionSESE
Submission TypeTraditional
Device ClassClass U

Regulatory Classification

Identification

Intended as a physical barrier to cover the wound and provide a moist wound environment. Intended to be left on wounds after topical application.

Innolitics
Guidance Recalls

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