Cunningham Woodland, Inc.
Hyannis, MA, US
CUNNINGHAM WOODLAND, INC. appears in FDA device records in Hyannis, MA. FDA records list 10 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 10 510(k) clearances for Cunningham Woodland, Inc. between 1981 and 1983. The busiest year on record is 1981, with 7. The most recent is 1983, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 7 |
| 1982 | 2 |
| 1983 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K823527 | SUBCLAVIAN INSERTION KIT | FMF | Substantially Equivalent | |
| K813286 | PRE-PACK TENS | GDY | Substantially Equivalent | |
| K813519 | NON-ABSORBENT TOWELS | KME | Substantially Equivalent | |
| K813284 | VENOUS CANNULA TRAY | DWS | Substantially Equivalent | |
| K811091 | MINOR DRESSING TRAY | LDQ | Substantially Equivalent | |
| K811090 | MAJOR DRESSING TRAY | LDQ | Substantially Equivalent | |
| K811089 | ONE STEP PREP KIT | LDQ | Substantially Equivalent | |
| K811088 | DRESSING TRAY MERCY HOSPITAL | LDQ | Substantially Equivalent | |
| K811087 | MIKA SKIN SCRUB TRAY PRE OPERATIVE W/GEL | FSM | Substantially Equivalent | |
| K811086 | SUTURE REMOVAL SET(DISPLSABLE) | KDD | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1219659 | 1219659 | CUNNINGHAM WOODLAND, INC. | 350 B Kidds Hill Rd, Hyannis, MA 02601 US | 2026 | and 2 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered
- GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered
- KMEBedding, Disposable, Medical
- DXCClamp, Vascular
- DWPDilator, Vessel, Surgical
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- HTDForceps
- GENForceps, General & Plastic Surgery
- HCZForceps, Surgical, Gynecological
- GDYGauze/Sponge, Internal, X-Ray Detectable
- DWSInstruments, Surgical, Cardiovascular
- KDDKit, Surgical Instrument, Disposable
- GCJLaparoscope, General & Plastic Surgery
- GZTRetractor, Self-Retaining, For Neurosurgery
- HAERongeur, Manual
- LRWScissors, General, Surgical
- FMFSyringe, Piston
- FSMTray, Surgical, Instrument
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain