Skip to the page

Data / Medical devices / United States / Cunningham Woodland, Inc.

Cunningham Woodland, Inc.: FDA-registered device maker in Hyannis, MA, United States, 7 510(k) clearances

Cunningham Woodland, Inc. is registered with the FDA (registration 1219659) in Hyannis, MA, United States. It lists 12 device types. The FDA files 7 510(k) clearances under its listings, the newest dated August 31, 2010. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
1219659
Address
350 B Kidds Hill Rd, Hyannis, MA, United States, 02601
Owner or operator
CUNNINGHAM WOODLAND, INC. (1219659)
Roles
Repackager or relabeler
First device listed
September 27, 2016
Registered through
2026
Brand names listed
Cunningham Woodland, Inc, Cunningham Woodland, Inc.

Devices it lists

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
August 31, 2010K100518INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054DWPSubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
December 3, 2009K092840INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICALHCZSubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
October 26, 2009K092544INSTRUMED VASCULAR CLAMPSDXCSubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
August 8, 2008K081651INSTRUMED RONGEURHAESubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
August 2, 2007K071771INSTRUMED RETRACTORSGZTSubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
April 16, 2004K040855INSTRUMED LAPAROSCOPE AND ACCESSORIESGEISubstantially EquivalentInstrumed International, Inc.accessdata.fda.gov
June 24, 1998K974594SEMKIN BIPOLAR FORCEPHTDSubstantially EquivalentTitan Mfg., Inc.accessdata.fda.gov

Compare with other makers

Updated August 31, 2010. 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.