Inovo, Inc.
Inovo, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2014, with 3 FDA device recalls on record.
Top product codes for Inovo, Inc.
FDA recalls by Inovo, Inc.
- Z-2099-2019 — Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxygen from an oxygen tank and only deliver oxygen as the patient inhales, resulting in greater efficiency and cost saving ratios.
- Z-0407-2018 — PURE OXYGEN CONCENTRATOR, CHAD Drive, Models CH5000 and CH5000S
- Z-0760-2017 — INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen refill machine that you can attach to an oxygen concentrator to refill portable oxygen cylinders.
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 Inovo, Inc.
- K141967 — PUREFILL OXYGEN COMPRESSOR
- K113111 — CHAD THERAPEUTIC EVOLUTION ELECTRONIC OXYGEN CONSERVER WITH MOTION
- K103392 — CHAD THERAPEUTIC EVOLUTION ELECTRONIC OXYGEN CONSERVER
- K060751 — INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR
- K051540 — INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR
- K031983 — INOVO, INC, ECONOMIZER CONSERVING REGULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.