Epimed International
Epimed International holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2024, with 7 FDA device recalls on record.
Top product codes for Epimed International
FDA recalls by Epimed International
- Z-1849-2020 — R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
- Z-1850-2020 — R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)00818788022127 - Product Usage:The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
- Z-2312-2021 — NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile
- Z-2313-2021 — NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile
- Z-0088-2018 — COUDE Blunt Nerve Block Needle, 10 units, 0.71mm (22 Ga) x 152mm, Each Unit Contains One Blunt Nerve Block Needle and One Wing, Sterile
- Z-0087-2018 — RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter
- Z-0089-2018 — TUOHY Epidural Needle, 20g x 3.5in(8.9cm) TW, 10 units, Calibrated, Plastic Hub, Fixed Wing, Sterile, Rx only
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 Epimed International
Data sourced from openFDA. This site is unofficial and independent of the FDA.