Keymed (Medical & Industrial Equipment), Ltd.

FDA Regulatory Profile

Keymed (Medical & Industrial Equipment), Ltd. has 0 FDA recalls, 3 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 5, 2015 · VAI
Latest 510(k)
Apr 6, 2020

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 5, 2015Southend-On-Sea, United KingdomDevicesVoluntary Action Indicated (VAI)1000162602
Oct 20, 2011Southend-On-Sea, United KingdomDevicesVoluntary Action Indicated (VAI)1000162602
Nov 6, 2008Southend-On-Sea, United KingdomDevicesVoluntary Action Indicated (VAI)1000162602

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K193250Irrigation Tubing with CO2 or AirApr 6, 2020
K100899OLYMPUS ENDOSCOPIC FLUSHING PUMP, MODEL OPF-2Sep 13, 2010
K011725OLYMPUS SUCTION PUMP, MODEL KV-5Aug 31, 2001
K000948OLYMPUS ENDOSCOPIC FLUSHING PUMP MODEL OFP-1May 12, 2000
K962528OLYMPUS MOBILE CHAIR/COUCHDec 12, 1996
K930852OLYMPUS SUCTION PUMP MODEL KV-4Mar 31, 1994
K881478MODIFIED KEYMED FLEXIBLE ESOPHAGEAL DILATORSSep 14, 1988