FDA.reportPublic FDA data

CUNNINGHAM WOODLAND, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
12196591219659CUNNINGHAM WOODLAND, INC.1Y2026-01-01350 B Kidds Hill Rd Hyannis MA US 02601

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
302151286195616K974594SEMKIN BIPOLAR FORCEPHTD1998-06-24
302151626387356K100518INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054DWP2010-08-31
302151455867406K092840INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICALHCZ2009-12-03
302151787563889K092544INSTRUMED VASCULAR CLAMPSDXC2009-10-26
302151934295824K081651INSTRUMED RONGEURHAE2008-08-08
302151012990323K071771INSTRUMED RETRACTORSGZT2007-08-02
302151380530051K040855INSTRUMED LAPAROSCOPE AND ACCESSORIESGEI2004-04-16
302151183279454
302151317764488
302152002861561
302152071731240

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DWP12010-08-31
HCZ12009-12-03
DXC12009-10-26
HAE12008-08-08
GZT12007-08-02
GEI12004-04-16
HTD11998-06-24

PMN#