Reflow Medical
Reflow Medical holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2021, with 1 FDA device recall on record.
Top product codes for Reflow Medical
FDA recalls by Reflow Medical
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 Reflow Medical
- K210188 — coraCross
- K200094 — speX LP Support Catheter
- K193596 — Wingman 14, Wingman 14C, Wingman 18, Wingman 35
- K193012 — speX Support Catheter
- K151880 — Wingman Crossing Catheter
- K141649 — SPEX SUPPORT CATHETER
- K141547 — WINGMAN EXTENDABLE TIP SUPPORT CATHETER
- K132420 — WINGMAN EXTENDABLE TIP SUPPORT CATHETER
- K120178 — WINGMAN EXTENDABLE TIP SUPPORT CATHETER
- K101479 — WINGMAN EXTENDABLE TIP SUPPORT CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.