Katecho LLC

Country not established FDA establishment FEI 1930027

Devices: 26
Registrations: FDA
FDA recalls: 0

What Katecho LLC makes

Katecho LLC manufactures disposable and reusable electrodes for transcutaneous electrical nerve stimulation (TENS), defibrillation/pacing, and pediatric emergency use, including sterile and non-sterile variants. Their product line also includes mesh materials for surgical applications, such as K-Apatite mesh in varying mesh sizes.

The company’s devices are regulated under FDA Class II and Class III classifications, with most products cleared via the 510(k) pathway. Their products are listed in the FDA’s 510(k) database, and the company is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue26

Newest first, rows 1-26 of 26

Search and filter all 26 devices

K-Sterile Tens Electrodes Ref K900997

Class II

Active 510(k) 510(k) II
K-Defib/Pace Pediatric Electrode Ref K934692

Class III

Active 510(k) 510(k) III
K-Stim Clear Ref K922202

Class II

Active 510(k) 510(k) II
K-Defib/Pace Electrode Ref K914955

Class II

Active 510(k) 510(k) II
K-Free Ref K912587

Class II

Active 510(k) 510(k) II
Km-10 Tens Electrode Ref K000870

Class II

Active 510(k) 510(k) II
K-Apatite 20-40 Mesh K-Apatite 40-60 Ref K843557

Class II

Active 510(k) 510(k) II
K-Defib/Pace, Model Kdp-60A Ref K002806

Class III

Active 510(k) 510(k) III
K-Defib/Pace Multifuction Pediatric Electrode, Model Kdp-70A Ref K003228

Class III

Active 510(k) 510(k) III
K-Defib/Pace Pediatric Electrode Ref K954504

Class III

Active 510(k) 510(k) III
K-Stim Ref K913031

Class II

Active 510(k) 510(k) II
Km-30 Tens Electrode Ref K010543

Class II

Active 510(k) 510(k) II
K-Defib/Pace Adult Electrode Model Number Kdp-60 Ref K981737

Class III

Active 510(k) 510(k) III
K-Defib/Pace Carbon Electrode Ref K926175

Class II

Active 510(k) 510(k) II
K-Mesh Ref K843829

Not classified

Active 510(k) 510(k) —
Gel-Tac Ref K915328

Class II

Active 510(k) 510(k) II
K-Snap Ref K940586

Class II

Active 510(k) 510(k) II
Low Back Strip (Or) K-Back Ref K912381

Class II

Active 510(k) 510(k) II
K-Stik Defibrillation Pads Ref K863899

Class II

Active 510(k) 510(k) II
K-Defib/Pace Radiolucent Adult Electrode, Model Krt-60 Ref K991007

Class III

Active 510(k) 510(k) III
Pediatric Defib K-Pads Ref K935083

Class II

Active 510(k) 510(k) II
K-Disperse Ref K921679

Class II

Active 510(k) 510(k) II
K-Defib/Pace Adult Electrode, Model Kdp-80 Ref K993745

Class III

Active 510(k) 510(k) III
K-Klip Ref K940801

Class II

Active 510(k) 510(k) II
K-Defib/Pace Adult Electrode, Model Kdp-85 Ref K012404

Class II

Active 510(k) 510(k) II
Defib K-Pads Ref K895662

Class II

Active 510(k) 510(k) II

Rows 1-26 of 26

Company details

FDA FEI number: 1930027
Address: 4020 GANNETT AVENUE., DES MOINES, IA, 50321

Frequently asked questions

How many devices does KATECHO LLC have in the registry?

The registry currently lists 26 devices for KATECHO LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list KATECHO LLC's devices?

Among its 26 most recently registered devices, KATECHO LLC has devices listed in FDA 510(k) (26 devices).

What risk classes do KATECHO LLC's devices fall under?

Among its 26 most recently registered devices, the classes recorded for KATECHO LLC's devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from KATECHO LLC in the registry?

The most recently registered devices listed for KATECHO LLC include K-STERILE TENS ELECTRODES, K-DEFIB/PACE PEDIATRIC ELECTRODE, K-STIM CLEAR and K-DEFIB/PACE ELECTRODE.

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.

What Katecho LLC makes

Catalogue26

K-Sterile Tens Electrodes Ref K900997

K-Defib/Pace Pediatric Electrode Ref K934692

K-Stim Clear Ref K922202

K-Defib/Pace Electrode Ref K914955

K-Free Ref K912587

Km-10 Tens Electrode Ref K000870

K-Apatite 20-40 Mesh K-Apatite 40-60 Ref K843557

K-Defib/Pace, Model Kdp-60A Ref K002806

K-Defib/Pace Multifuction Pediatric Electrode, Model Kdp-70A Ref K003228

K-Defib/Pace Pediatric Electrode Ref K954504

K-Stim Ref K913031

Km-30 Tens Electrode Ref K010543

K-Defib/Pace Adult Electrode Model Number Kdp-60 Ref K981737

K-Defib/Pace Carbon Electrode Ref K926175

K-Mesh Ref K843829

Gel-Tac Ref K915328

K-Snap Ref K940586

Low Back Strip (Or) K-Back Ref K912381

K-Stik Defibrillation Pads Ref K863899

K-Defib/Pace Radiolucent Adult Electrode, Model Krt-60 Ref K991007

Pediatric Defib K-Pads Ref K935083

K-Disperse Ref K921679

K-Defib/Pace Adult Electrode, Model Kdp-80 Ref K993745

K-Klip Ref K940801

K-Defib/Pace Adult Electrode, Model Kdp-85 Ref K012404

Defib K-Pads Ref K895662

Company details

Frequently asked questions