Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1219659

FEI Number

1219659

Entity Name

CUNNINGHAM WOODLAND, INC.

City/State/Country

Hyannis, MA, US

Establishment Address

350 B Kidds Hill Rd, Hyannis, MA 02601, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CUNNINGHAM WOODLAND, INC. (Owner Number: 1219659)

Owner / Operator Contact Address

350 B Kidds Hill Road, --, Hyannis, MA 02601, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K081651

PMA Number

N/A

All Registered Proprietary Names

Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc Cunningham Woodland, Inc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DWP	Dilator, Vessel, Surgical	Cardiovascular	Class 2	870.4475	2016-09-28
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2016-09-28
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2016-09-28
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2016-09-28
GCX	Apparatus, Suction, Operating-Room, Wall Vacuum Powered	General Hospital	Class 2	880.6740	2016-09-28
GCJ	Laparoscope, General & Plastic Surgery	Gastroenterology, Urology	Class 2	876.1500	2016-09-28
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2016-09-28
HCZ	Forceps, Surgical, Gynecological	Obstetrics/Gynecology	Class 2	884.4530	2016-09-28
GZT	Retractor, Self-Retaining, For Neurosurgery	Neurology	Class 2	882.4800	2016-09-28
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2016-09-28
HAE	Rongeur, Manual	Neurology	Class 2	882.4840	2016-09-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CUNNINGHAM WOODLAND, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K810894	American Edwards Laboratories	FOGARTY FLEXIBLE CALIBRATOR	1981-05-15
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0027-2009	Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa	2	Applied Medical, Lap Banding Kit, REF: K0398 Contains: (2) C0Q04, 5x100mm Threaded Kii Access System (1) C0604, 15x100mm Non-Threaded Separator System w/Universal Seal, for laparoscopic procedures.
Z-0028-2009	Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa	2	Applied Medical, Lap Banding Kit, REF: K0406 Contains: (1) C0658, 11x100mm Threaded Shielded Trocar w/Universal Seal (1) C0522, 5x100mm Threaded Premium Flat Blade (1) C2202, 150mm Insufflation needle (1) C0605, 15x100mm Threaded Separator Access System (1) CB030, 5mm x 35cm Direct Drive Disposable Scissors (2) C4120, 5mm x 38cm Direct Drive Grasper Reposable Cartridge, for laparoscopic procedures.
Z-0029-2009	Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa	2	Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains: (1) C0Q04, 5x100mm Threaded Kii Access System (1) C0130, 12x100mm Optical Separator System, Non-handled (2) C0Q10, 5x100mm Threaded Kii Cannula and Seal (1) C0605, 15mmx100mm Threaded Cannula System, for laparoscopic procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1219659. Last updated year: 2026. Please use registration number 1219659 when referencing this establishment in official correspondence.