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Data / Medical devices / United States / J & J Instruments, LLC

J & J Instruments, LLC: FDA-registered device maker in Northbrook, IL, United States, 1 510(k) clearance

J & J Instruments, LLC is registered with the FDA (registration 2246990) in Northbrook, IL, United States. It lists 66 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 6, 2012. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch J & J Instruments, LLC
FDA registration number
2246990
Address
2501 Sanders Rd, Northbrook, IL, United States, 60062
Owner or operator
J&J Instruments (2246990)
Roles
Complaint file establishment, Specification developer
First device listed
December 3, 2007
Registered through
2027
Brand names listed
Carver, Cleoid Discoid, J&J Instruments, Julius Wirth, OPENING AND PLACER TOOL

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, Implant, Dental, EndosseousNDP1Specification developeraccessdata.fda.gov
Accessories, Retractor, DentalEIF1Specification developeraccessdata.fda.gov
Aligner, Bracket, OrthodonticECQ1Specification developeraccessdata.fda.gov
Bone MillLYS1Specification developeraccessdata.fda.gov
Burnisher, OperativeEKJ1Specification developeraccessdata.fda.gov
Cannula, SinusKAM1Specification developeraccessdata.fda.gov
Capsule, Dental, AmalgamDZS1Specification developeraccessdata.fda.gov
Carrier, Amalgam, OperativeEKI1Specification developeraccessdata.fda.gov
Carver, Dental Amalgam, OperativeEKH1Specification developeraccessdata.fda.gov
Carver, Wax, DentalEIK1Specification developeraccessdata.fda.gov
Chisel (Osteotome)KDG1Specification developeraccessdata.fda.gov
Chisel, Bone, SurgicalEML1Specification developeraccessdata.fda.gov
Clamp, Eyelid, OphthalmicHOD1Specification developeraccessdata.fda.gov
Clamp, Rubber DamEEF1Specification developeraccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Specification developeraccessdata.fda.gov
Curette, EarJYG1Specification developeraccessdata.fda.gov
Curette, OperativeEKE1Specification developeraccessdata.fda.gov
Curette, PeriodonticEMS1Specification developeraccessdata.fda.gov
Cutter, SurgicalFZT1Specification developeraccessdata.fda.gov
Dam, RubberEIE1Specification developeraccessdata.fda.gov
Elevator, Surgical, DentalEMJ1Specification developeraccessdata.fda.gov
Excavator, Dental, OperativeEKC1Specification developeraccessdata.fda.gov
Explorer, OperativeEKB1Specification developeraccessdata.fda.gov
File, Bone, SurgicalEMI1Specification developeraccessdata.fda.gov
ForcepsHTD1Specification developeraccessdata.fda.gov
Forceps, Articulation PaperEFK1Specification developeraccessdata.fda.gov
Forceps, Dressing, DentalEFL1Specification developeraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Specification developeraccessdata.fda.gov
Gag, MouthKBN1Specification developeraccessdata.fda.gov
Gauge, Depth, Instrument, DentalEIL1Specification developeraccessdata.fda.gov
Handle, Instrument, DentalEJB1Specification developeraccessdata.fda.gov
Handle, ScalpelGDZ1Specification developeraccessdata.fda.gov
Hemostat, SurgicalEMD1Specification developeraccessdata.fda.gov
Hoe, PeriodonticEMQ1Specification developeraccessdata.fda.gov
Holder, Needle; OrthopedicHXK1Specification developeraccessdata.fda.gov
Instrument, Cast Application/Removal, ManualLGG1Specification developeraccessdata.fda.gov
Instrument, Cutting, OperativeEKD1Specification developeraccessdata.fda.gov
Instrument, Filling, Plastic, DentalEIY1Specification developeraccessdata.fda.gov
Instrument, Ligature Tucking, OrthodonticECP1Specification developeraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Specification developeraccessdata.fda.gov
Instruments, Dental HandDZN1Specification developeraccessdata.fda.gov
Knife, Margin Finishing, OperativeEJZ1Specification developeraccessdata.fda.gov
Knife, PeriodonticEMO1Specification developeraccessdata.fda.gov
MalletHXL1Specification developeraccessdata.fda.gov
Mirror, MouthEAX1Specification developeraccessdata.fda.gov
PinwheelGWY1Specification developeraccessdata.fda.gov
Plier, OrthodonticJEX1Specification developeraccessdata.fda.gov
Pliers, OperativeEJY1Specification developeraccessdata.fda.gov
Plugger, Root Canal, EndodonticEKR1Specification developeraccessdata.fda.gov
Preparer, Root Canal EndodonticEKQ1Specification developeraccessdata.fda.gov
Probe, PeriodonticEIX1Specification developeraccessdata.fda.gov
Pusher, Band, OrthodonticECS1Specification developeraccessdata.fda.gov
Remover, CrownEIS1Specification developeraccessdata.fda.gov
Retractor, All TypesEIG1Specification developeraccessdata.fda.gov
Scaler, PeriodonticEMN1Specification developeraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Specification developeraccessdata.fda.gov
Scraper, TongueLCN1Complaint file establishmentaccessdata.fda.gov
Setter, Band, OrthodonticECR1Specification developeraccessdata.fda.gov
Spatula, Surgical, General & Plastic SurgeryGAF1Specification developeraccessdata.fda.gov
Speculum, EntEPY1Specification developeraccessdata.fda.gov
Speculum, Vaginal, MetalHDF1Specification developeraccessdata.fda.gov
Syringe, CartridgeEJI2Specification developeraccessdata.fda.gov
Syringe, Irrigating (Non Dental)KYZ1Specification developeraccessdata.fda.gov
Tray, Impression, PreformedEHY1Specification developeraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Specification developeraccessdata.fda.gov
Tube, Ear SuctionJZF1Specification developeraccessdata.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 6, 2012K120659HU-FRIEDY DENTAL CARTRIDGE SYRINGEEJISubstantially EquivalentHu-Friedy Mfg. Co., LLCaccessdata.fda.gov

Compare with other makers

Updated November 6, 2012. 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.