Cytrellis Biosystems, Inc.
Cytrellis Biosystems, Inc. holds FDA 510(k) medical device clearances, first cleared 2021, most recent 2025, with 2 FDA device recalls on record.
Top product codes for Cytrellis Biosystems, Inc.
FDA recalls by Cytrellis Biosystems, Inc.
- Z-2393-2023 — ellacor System with Micro-Coring Technology-Indicated for use by medical professionals for the treatment of moderate and severe wrinkles in the mid and lower face in adults aged 22 years or older with Fitzpatrick skin types I-IV. Model #: Gen 4
- Z-1648-2023 — Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for the treatment of moderate and severe wrinkles in the mid and lower face. Model #: Gen 4
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Cytrellis Biosystems, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.