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Data / Medical devices / China / Planet (anhui) Medical Products Co., Ltd

Planet (anhui) Medical Products Co., Ltd: FDA-registered device maker in Chuzhou Anhui, China, 2 510(k) clearances

Planet (anhui) Medical Products Co., Ltd is registered with the FDA (registration 3007187674) in Chuzhou Anhui, China. It lists 30 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 12, 2020. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Planet (anhui) Medical Products Co., Ltd
FDA registration number
3007187674
Address
No. 2066 West Jianshe Road, Hi-tech Zone, Chuzhou Anhui, China, 239300
Owner or operator
Planet (Anhui) Medical Products Co., Ltd (10078698)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
November 2, 2020
Registered through
2026
Brand names listed
0.38” x 1.5”Junior Adhesive Strips bulk, 1-470-001 2x4 XLG FABRIC BDGS 50/BX, 1-470G 2x4 XLG FABRIC BDGS 50/BX, 1.5"X3" Knuckle Fabric Heavy Woven Bandae Bulk, 1.5x3" Knuckle Fabric Bdg Bulk 3,300/CA, 1.75x2" Fingertip Fab Bdg Bulk, 1.75x3" Heavy Woven XL Fingertip Bdg, 1/2"x5yd Adhesive Tape 2/Bx and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Contract manufactureraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Contract manufactureraccessdata.fda.gov
Bandage, ElasticFQM1Contract manufactureraccessdata.fda.gov
Bandage, Liquid, Skin ProtectantNEC1Contract manufactureraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Contract manufactureraccessdata.fda.gov
Container, SharpsMMK2Repackager or relabeleraccessdata.fda.gov
Cotton, RollEFN1Contract manufacturer, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Cover, Shoe, Operating-RoomFXP1Contract manufactureraccessdata.fda.gov
Depressor, Tongue, Non-SurgicalFMA1Contract manufactureraccessdata.fda.gov
Dressing, CompressionMHW1Contract manufactureraccessdata.fda.gov
Dressing, Wound, DrugFROUContract manufacturer, Manufactureraccessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or BiologicNAE1Contract manufacturer, Manufactureraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Contract manufacturer, Manufactureraccessdata.fda.gov
Dressing, Wound, OcclusiveNAD1Contract manufacturer, Manufactureraccessdata.fda.gov
Finger CotLZB1Contract manufactureraccessdata.fda.gov
First Aid Kit With DrugLRRNContract manufactureraccessdata.fda.gov
First Aid Kit Without DrugOHO1Contract manufacturer, Manufactureraccessdata.fda.gov
ForcepsHTD1Contract manufactureraccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Contract manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Contract manufactureraccessdata.fda.gov
Mouthpiece, BreathingBYP1Contract manufactureraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Contract manufactureraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Contract manufactureraccessdata.fda.gov
Pad, EyeHMP1Contract manufacturer, Manufactureraccessdata.fda.gov
Sling, ArmILI1Contract manufactureraccessdata.fda.gov
Snake Bite Suction KitKYP1Contract manufactureraccessdata.fda.gov
Spill KitPXG1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Contract manufactureraccessdata.fda.gov
Strip, Temperature, Forehead, Liquid CrystalKPD2Contract manufactureraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Contract manufacturer, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
November 12, 2020K201523Sharps containerMMKSubstantially EquivalentZhejiang Gongdong Medical Technology Co., Ltd.accessdata.fda.gov
October 19, 2020K200821anti-bacterial bandageFROSubstantially EquivalentPlanet (Suzhou) Medical Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 12, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.