Pinook USA
Pinook USA holds FDA 510(k) medical device clearance, cleared in 2014, with 2 FDA device recalls on record.
Top product codes for Pinook USA
FDA recalls by Pinook USA
- Z-0177-2014 — Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen the abdominal muscles.
- Z-0176-2014 — Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.
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 Pinook USA
Data sourced from openFDA. This site is unofficial and independent of the FDA.