Shandong Weigao Group Medical Polymer Co., Ltd.

FDA Regulatory Profile

Shandong Weigao Group Medical Polymer Co., Ltd. has 0 FDA recalls, 2 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 21, 2016 · NAI
Latest 510(k)
Mar 23, 2023

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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
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 21, 2016Weihai, ChinaDevicesNo Action Indicated (NAI)3007084575
Apr 12, 2012Weihai, ChinaDevicesNo Action Indicated (NAI)3007084575

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
K212207Sterile Hypodermic Syringe for Single UseMar 23, 2023
K212920Sterile Safety Syringe with Needle for Single Use, Sterile Safety Hypodermic Needle for Single…Mar 11, 2022
K102741ENTERAL FEEDING BAG AND SETSNov 8, 2011
K102328BLUNT FILL NEEDLE AND BLUNT PLASTIC CANNULAMay 13, 2011
K081241WEIGAO EMPTY CARTRIDGE SYRINGESep 8, 2008
K072739JIERUI SYRINGES AND NEEDLESMar 21, 2008
K073127BLOOD COLLECTION NEEDLE, MODEL 20G 21G 22GDec 20, 2007