Turbett Surgical, Inc.
Turbett Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2021, with 3 FDA device recalls on record.
Top product codes for Turbett Surgical, Inc.
FDA recalls by Turbett Surgical, Inc.
- Z-1037-2023 — Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
- Z-1038-2023 — Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
- Z-1501-2022 — Turbett Surgical Container, TS1500
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 Turbett Surgical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.