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Cunningham Woodland, Inc.

Country not established FDA establishment FEI 1219659

Devices
10
Registrations
FDA
FDA recalls
0

What Cunningham Woodland, Inc. makes

Cunningham Woodland, Inc. manufactures single-use medical trays and kits for preoperative preparation, cannulation, and wound care, including pre-packaged transcutaneous electrical nerve stimulation (TENS) units, venous cannula trays, and subclavian insertion kits. Their product line also includes dressing trays (minor and major), suture removal sets, non-absorbent towels, and preoperative skin scrub trays with gel. These items are designed for surgical and procedural environments to streamline sterile field setup and patient care.

The company’s devices are classified under FDA categories Class I and Class II, with regulatory clearance obtained through the 510(k) pathway. Products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

  • Pre-Pack Tens Ref K813286

    Class I
    Active 510(k) 510(k) I

  • Venous Cannula Tray Ref K813284

    Class I
    Active 510(k) 510(k) I

  • One Step Prep Kit Ref K811089

    Not classified
    Active 510(k) 510(k) —

  • Subclavian Insertion Kit Ref K823527

    Class II
    Active 510(k) 510(k) II

  • Mika Skin Scrub Tray Pre Operative W/Gel Ref K811087

    Class I
    Active 510(k) 510(k) I

  • Dressing Tray Mercy Hospital Ref K811088

    Not classified
    Active 510(k) 510(k) —

  • Minor Dressing Tray Ref K811091

    Not classified
    Active 510(k) 510(k) —

  • Major Dressing Tray Ref K811090

    Not classified
    Active 510(k) 510(k) —

  • Non-Absorbent Towels Ref K813519

    Class I
    Active 510(k) 510(k) I

  • Suture Removal Set(Displsable) Ref K811086

    Class I
    Active 510(k) 510(k) I

Company details

FDA FEI number
1219659
Address
350 B Kidds Hill Rd, Hyannis, MA, 02601

Frequently asked questions

How many devices does CUNNINGHAM WOODLAND, INC. have in the registry?

The registry currently lists 10 devices for CUNNINGHAM WOODLAND, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list CUNNINGHAM WOODLAND, INC.'s devices?

Among its 10 most recently registered devices, CUNNINGHAM WOODLAND, INC. has devices listed in FDA 510(k) (10 devices).

What risk classes do CUNNINGHAM WOODLAND, INC.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for CUNNINGHAM WOODLAND, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from CUNNINGHAM WOODLAND, INC. in the registry?

The most recently registered devices listed for CUNNINGHAM WOODLAND, INC. include PRE-PACK TENS, VENOUS CANNULA TRAY, ONE STEP PREP KIT and SUBCLAVIAN INSERTION KIT.

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.