FDA Import Refusals: Devices — Page 8

139,705 import refusals total

Browse FDA import refusals in the Devices category, by firm, country and refusal date, from official FDA import records. RegDataLab tracks 139,705 import refusals from official FDA sources, updated on an ongoing basis.

FDA Import Refusals: Devices (page 8 of 2,795)
Import refusalsDetails
1FX-3169029-1/20002/1D — Q-Med ABSep 18, 2026 — SE
336-4388706-6/1690002/1 — Intercos Europe S.P.ASep 17, 2026 — IT
336-4388706-6/1740002/1 — Intercos Europe S.P.ASep 17, 2026 — IT
336-7671601-8/30001/1 — Abbott Vascular IncSep 17, 2026 — US
1FX-1166477-9/30002/1J — UNKNOWNSep 17, 2026 — GT
1FX-1166477-9/30002/1K — SINOZENITH CO., LIMITEDSep 17, 2026 — CN
1FX-3129606-5/30002/1E — JIANGSU ZHENGKANG MEDICAL APPARASep 17, 2026 — CN
1FX-3177504-3/30002/1F — Laboratorio Y Drogueria Qualipharm, S.A.Sep 17, 2026 — GT
1FX-3177504-3/30002/1G — CHANGZHOU HUICHUN MEDICAL EQUIPMENT CO LTDSep 17, 2026 — CN
1FX-3177504-3/30002/1H — CHANGZHOU HUICHUN MEDICAL EQUIPMENT CO LTDSep 17, 2026 — CN
1FX-5454514-1/10002/1 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/3 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/4 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/6 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/8 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/9 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/10 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/2 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/5 — Odontit SaSep 17, 2026 — AR
1FX-5454514-1/10002/7 — Odontit SaSep 17, 2026 — AR
SCS-7138565-0/10002/1 — PLASTIC PLUS LTDSep 17, 2026 — CA
N6J-0007609-2/10002/1 — JEISYS MEDICAL INCSep 17, 2026 — KR
336-7671601-8/20001/1 — Abbott Vascular IncSep 17, 2026 — US
336-7671601-8/10001/1 — Abbott Vascular IncSep 17, 2026 — US
AD1-0947868-6/10002/1 — SUNWA LTD.Sep 16, 2026 — JP
AD1-0948086-4/10001/1 — Garaventa (Canada), Ltd.Sep 16, 2026 — CA
AD1-0948091-4/10001/1 — Garaventa (Canada), Ltd.Sep 16, 2026 — CA
AEK-9592344-5/10002/1 — MAYPHARMSep 16, 2026 — KR
AEK-9592353-6/10002/1B — Q-Med ABSep 16, 2026 — SE
AEK-9592353-6/10002/1C — Q-Med ABSep 16, 2026 — SE
AEK-9592353-6/10002/1D — Daehan NupharmSep 16, 2026 — KR
AEK-9592346-0/10002/1 — Q-Med ABSep 16, 2026 — SE
AEK-9592363-5/10002/1 — QUIVER MEDIC INC.Sep 16, 2026 — KR
AEK-9592363-5/20002/1 — PharmaresearchSep 16, 2026 — KR
AEK-9592363-5/30002/1 — Allergan Industrie SASSep 16, 2026 — FR
AEK-9592363-5/50002/1C — UNKNOWNSep 16, 2026 — KR
SCS-3486555-8/80002/1 — Spectrum Medical Ltd.Sep 16, 2026 — GB
SCS-3882674-7/10002/1 — TOP SYRINGE MFG COSep 16, 2026 — IN
SCS-3882674-7/20002/1 — TOP SYRINGE MFG COSep 16, 2026 — IN
SCS-3882674-7/30002/1 — TOP SYRINGE MFG COSep 16, 2026 — IN
SCS-3882674-7/40002/1 — TOP SYRINGE MFG COSep 16, 2026 — IN
1FX-4009707-4/10002/1 — Prollenium Medical Technologies Inc.Sep 15, 2026 — CA
8T9-0049300-4/10002/1 — ELESTA SRLSep 15, 2026 — IT
823-0226399-9/10001/1 — Metrex Research, LLC.Sep 15, 2026 — US
1FX-5969272-3/10002/1 — JOHNSON AND JOHNSON VISION CARESep 15, 2026 — IN
AEK-0899175-3/10002/1A — KORESTETICSSep 15, 2026 — KR
AEK-0899175-3/10002/1B — KORESTETICSSep 15, 2026 — KR
AEK-2087941-6/10002/1 — Q-Med ABSep 14, 2026 — SE
1FX-1775131-5/20001/1 — COMEM NATURAL JSCSep 14, 2026 — VN
1FX-1267848-9/20002/1A — Q-Med ABSep 14, 2026 — SE
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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.