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Data / Medical devices / China / Guangzhou Aquila Precise Tools Limited

Guangzhou Aquila Precise Tools Limited: FDA-registered device maker in Guangzhou City Guangdong, China, 1 510(k) clearance

Guangzhou Aquila Precise Tools Limited is registered with the FDA (registration 3010388970) in Guangzhou City Guangdong, China. It lists 28 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 9, 2012. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Guangzhou Aquila Precise Tools Limited
FDA registration number
3010388970
Address
Jinsiwei Industrial Zone, Dachongkou Village, Shawan Town Panyu District, Guangzhou City Guangdong, China, 511483
Owner or operator
Guangzhou Aquila Precise Tools Limited (10044682)
Roles
Contract manufacturer, Manufacturer
First device listed
July 14, 2013
Registered through
2027

Devices it lists

DeviceProduct codeClassRoleSource
Bit, DrillHTW1Contract manufacturer, Manufactureraccessdata.fda.gov
Bit, SurgicalGFG1Contract manufactureraccessdata.fda.gov
Blade, Saw, General & Plastic Surgery, SurgicalGFA1Manufactureraccessdata.fda.gov
Bone MillLYS1Contract manufacturer, Manufactureraccessdata.fda.gov
BroachHTQ1Contract manufactureraccessdata.fda.gov
CaliperKTZ1Contract manufacturer, Manufactureraccessdata.fda.gov
Driver, ProsthesisHWR1Contract manufactureraccessdata.fda.gov
Driver, Surgical, PinGFC1Contract manufacturer, Manufactureraccessdata.fda.gov
ExtractorHWB1Contract manufactureraccessdata.fda.gov
ForcepsHTD1Manufactureraccessdata.fda.gov
Guide, Surgical, InstrumentFZX1Contract manufacturer, Manufactureraccessdata.fda.gov
Helmet, SurgicalFXZ1Contract manufacturer, Manufactureraccessdata.fda.gov
ImpactorHWA1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, Cutting, OrthopedicHTZ1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE1Contract manufactureraccessdata.fda.gov
Instruments Designed For Press-Fit Osteochondral ImplantsQBO2Contract manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Contract manufactureraccessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH2Contract manufactureraccessdata.fda.gov
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH2Contract manufactureraccessdata.fda.gov
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH2Contract manufacturer, Manufactureraccessdata.fda.gov
Punch, SurgicalLRY1Manufactureraccessdata.fda.gov
RaspHTR1Contract manufacturer, Manufactureraccessdata.fda.gov
ReamerHTO1Contract manufacturer, Manufactureraccessdata.fda.gov
ScrewdriverHXX1Contract manufactureraccessdata.fda.gov
Stripper, SurgicalHRT1Manufactureraccessdata.fda.gov
Tap, BoneHWX1Contract manufactureraccessdata.fda.gov
TemplateHWT1Contract manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Contract 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 9, 2012K122765PERSONA NATURAL TIBIA BASEPLATESJWHSubstantially EquivalentZimmer, Inc.accessdata.fda.gov

Compare with other makers

Updated November 9, 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.