Axelgaard Mfg. Co., Ltd.

United Statesfrom the FDA registration address FDA establishment FEI 1000603528

Devices: 11
Registrations: FDA
FDA recalls: 0

Catalogue11

Newest first, rows 1-11 of 11

Search and filter all 11 devices

Electrical Nerve Stimulation(Tens) Electrodes Ref K852267

Active Regimes: 510(k) Registry: 510(k) Class:II
Pals Platinum Neurostimulation Electrodes Ref K132422

Active Regimes: 510(k) Registry: 510(k) Class:II
Ultrastim Kit Ref K013532

Active Regimes: 510(k) Registry: 510(k) Class:II
Valutrode Neurostimlation Electrodes Ref K130987

Active Regimes: 510(k) Registry: 510(k) Class:II
Ultrastim Electrode, Model US4040 Ref K000947

Active Regimes: 510(k) Registry: 510(k) Class:II
Transcutaneous Electric Nerve Stimulation (Tens) Ref K874469

Active Regimes: 510(k) Registry: 510(k) Class:II
Comfort Iontophoresis Electrodes/ Buffered Iontophoresis Electrode Treatment, Model Small DDS275, Medium DDM325, Large D Ref K080580

Active Regimes: 510(k) Registry: 510(k) Class:II
Valuetrode Ref K970426

Active Regimes: 510(k) Registry: 510(k) Class:II
Pals Neonatal Pediatric Ecg Electrode, Models PN100, PN200 Ref K000206

Active Regimes: 510(k) Registry: 510(k) Class:II
Everlast Neurostimulation Electrodes 2X 2, Model # EL2020 Ref K983741

Active Regimes: 510(k) Registry: 510(k) Class:II
Tens Pals Plus Ref K872976

Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-11 of 11

Company details

FDA FEI number: 1000603528
Address: 520 INDUSTRIAL WAY, FALLBROOK, CA, 92028

Frequently asked questions

How many devices does AXELGAARD MFG. CO., LTD. have in the registry?

The registry currently lists 11 devices for AXELGAARD MFG. CO., LTD.. Devices recorded under merged duplicate company entries are counted once.

Which registries list AXELGAARD MFG. CO., LTD.'s devices?

Among its 11 most recently registered devices, AXELGAARD MFG. CO., LTD. has devices listed in FDA 510(k) (11 devices).

What risk classes do AXELGAARD MFG. CO., LTD.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for AXELGAARD MFG. CO., LTD.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from AXELGAARD MFG. CO., LTD. in the registry?

The most recently registered devices listed for AXELGAARD MFG. CO., LTD. include ELECTRICAL NERVE STIMULATION(TENS) ELECTRODES, PALS PLATINUM NEUROSTIMULATION ELECTRODES, ULTRASTIM KIT and VALUTRODE NEUROSTIMLATION ELECTRODES.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.

Catalogue11

Electrical Nerve Stimulation(Tens) Electrodes Ref K852267

Pals Platinum Neurostimulation Electrodes Ref K132422

Ultrastim Kit Ref K013532

Valutrode Neurostimlation Electrodes Ref K130987

Ultrastim Electrode, Model US4040 Ref K000947

Transcutaneous Electric Nerve Stimulation (Tens) Ref K874469

Comfort Iontophoresis Electrodes/ Buffered Iontophoresis Electrode Treatment, Model Small DDS275, Medium DDM325, Large D Ref K080580

Valuetrode Ref K970426

Pals Neonatal Pediatric Ecg Electrode, Models PN100, PN200 Ref K000206

Everlast Neurostimulation Electrodes 2X 2, Model # EL2020 Ref K983741

Tens Pals Plus Ref K872976

Company details

Frequently asked questions