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Data / Medical devices / United States / TPC Advanced Technology, Inc.

TPC Advanced Technology, Inc.: FDA-registered device maker in City Industry, CA, United States, 9 510(k) clearances

TPC Advanced Technology, Inc. is registered with the FDA (registration 2031508) in City Industry, CA, United States. It lists 44 device types. The FDA files 9 510(k) clearances under its listings, the newest dated September 10, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
2031508
FEI number
3001708019
Address
851. S. Lawson St., City Industry, CA, United States, 91748
Owner or operator
TPC ADVANCED TECHNOLOGY, INC. (9034634)
Roles
Repackager or relabeler
First device listed
July 30, 2002
Registered through
2027
Brand names listed
Bellagio Operatory Package, Dental handpiece, Infinity 5 Scanner, Laguna Hygiene Operatory Package, Laguna Operatory Package, Laguna Orthodontic Operatory Package, Laguna Swing Mount Operatory Package, MC3600CV Mirage Mobile Cart and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Repackager or relabeleraccessdata.fda.gov
Activator, Ultraviolet, For PolymerizationEBZ2Repackager or relabeleraccessdata.fda.gov
Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)KOQ1Repackager or relabeleraccessdata.fda.gov
Amalgamator, Dental, Ac-PoweredEFD1Repackager or relabeleraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Repackager or relabeleraccessdata.fda.gov
Cabinet, Table And Tray, AnesthesiaBRY1Repackager or relabeleraccessdata.fda.gov
Chair, Dental, With Operative UnitKLC1Repackager or relabeleraccessdata.fda.gov
Chair, Dental, Without Operative UnitNRU1Repackager or relabeleraccessdata.fda.gov
Chair, Surgical, Non-ElectricalFZK1Repackager or relabeleraccessdata.fda.gov
Cleaner, Ultrasonic, Medical InstrumentFLG1Repackager or relabeleraccessdata.fda.gov
Compressor, Air, PortableBTI2Repackager or relabeleraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Repackager or relabeleraccessdata.fda.gov
Cotton, RollEFN1Repackager or relabeleraccessdata.fda.gov
Cup, ProphylaxisEHK1Repackager or relabeleraccessdata.fda.gov
Dental Hygiene KitNXZ1Repackager or relabeleraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Repackager or relabeleraccessdata.fda.gov
Drill, Dental, IntraoralDZA1Repackager or relabeleraccessdata.fda.gov
Evacuator, Oral CavityEHZ1Repackager or relabeleraccessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKRNRepackager or relabeleraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Repackager or relabeleraccessdata.fda.gov
General Purpose Dental TrayOFX1Repackager or relabeleraccessdata.fda.gov
Handpiece, Air-Powered, DentalEFB1Repackager or relabeleraccessdata.fda.gov
Holder, Film, X-RayEGZ1Repackager or relabeleraccessdata.fda.gov
Illuminator, Radiographic-FilmIXC1Repackager or relabeleraccessdata.fda.gov
Indicator, Physical/Chemical Sterilization ProcessJOJ2Repackager or relabeleraccessdata.fda.gov
Instrument, Hand, Calculus RemovalELA1Repackager or relabeleraccessdata.fda.gov
Light, Fiber Optic, DentalEAY1Repackager or relabeleraccessdata.fda.gov
Light, Operating, DentalEAZ1Repackager or relabeleraccessdata.fda.gov
Non-Surgical GownOEA1Repackager or relabeleraccessdata.fda.gov
Portable Dental Operative UnitSJH1Repackager or relabeleraccessdata.fda.gov
Radiology Dental TrayOIK2Repackager or relabeleraccessdata.fda.gov
Respirator, SurgicalMSH2Repackager or relabeleraccessdata.fda.gov
Scaler, PeriodonticEMN1Repackager or relabeleraccessdata.fda.gov
Scaler, UltrasonicELC2Repackager or relabeleraccessdata.fda.gov
Scanner, ColorKZN2Repackager or relabeleraccessdata.fda.gov
Stand, Instrument, Ac-Powered, OphthalmicHMF1Repackager or relabeleraccessdata.fda.gov
Stool, Operating-RoomFZM1Repackager or relabeleraccessdata.fda.gov
Syringe, Restorative And Impression MaterialEID1Repackager or relabeleraccessdata.fda.gov
Tray, Fluoride, DisposableKMT1Repackager or relabeleraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Repackager or relabeleraccessdata.fda.gov
Unit, Operative DentalEIA1Repackager or relabeleraccessdata.fda.gov
Unit, Operative Dental, AccessoriesNRD1Repackager or relabeleraccessdata.fda.gov
Unit, Suction OperatoryEBR1Repackager or relabeleraccessdata.fda.gov
Wrap, SterilizationFRG2Repackager or relabeleraccessdata.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
September 10, 2026K254009Portable Dental Unit (PC 2630, OMC 2375CV, MC 3600CV)SJHSubstantially EquivalentLakong Medical Devices Co., Ltd.accessdata.fda.gov
August 7, 2026K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)EIASubstantially EquivalentLakong Medical Devices Co., Ltd.accessdata.fda.gov
November 28, 2018K180207Non-contact Infrared ThermometerFLLSubstantially EquivalentAlicn Medical (Shenzhen), Inc.accessdata.fda.gov
April 28, 2017K162258Self Sealing Sterilization PouchesFRGSubstantially EquivalentTianchang Jiarui Packaging Material Co., Ltd.accessdata.fda.gov
August 28, 2007K071485TPC ADVANCECAM INTRA ORAL CAMERA SYSTEM, MODEL AIC 888EIASubstantially EquivalentTpc Advanced Technology, Inc.accessdata.fda.gov
July 14, 2005K051547POWERMAX 25, MODEL PM25; POWERMAX 30, MODEL PM30ELCSubstantially EquivalentTpc Advanced Technology, Inc.accessdata.fda.gov
February 6, 2004K033213CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPSEFBSubstantially EquivalentCodent Technical Industry Co., Ltd.accessdata.fda.gov
June 12, 2002K020874ULTRA-LITE 5 TURBO LIGHT CURE UNITEBZSubstantially EquivalentRolence Ent., Inc.accessdata.fda.gov
October 10, 2000K001719Q-LUX PLASMA 100 LIGHT CURE UNITEBZSubstantially EquivalentRolence Enterprise Co. , Ltd.accessdata.fda.gov

Compare with other makers

Updated September 10, 2026. 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.