Multi-Med, Inc.
United StatesFDA applicant, unverified FDA FEI 1221765
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 75
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Enteral Feeding Container Ref K890424
Regimes: 510(k) Registry: 510(k)External Feeding Set For Pump Use Ref K890396
Regimes: 510(k) Registry: 510(k)Intravascular Administration Set Ref K891919
Regimes: 510(k) Registry: 510(k)Intravascular Administration Set Ref K890127
Regimes: 510(k) Registry: 510(k)Intravascular Administration Set Ref K891072
Regimes: 510(k) Registry: 510(k)Safety Subcutaneous Tissue Infusion Set Ref K120195
Regimes: 510(k) Registry: 510(k)Intravascular Administration Set Ref K890340
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1221765
- Address
- 26 Victoria Ct, Keene, NH, 03431
FDA recalls
2010
- 30 Aug 2010 Z-2506-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2507-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2508-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2509-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2510-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2511-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2512-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2513-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2514-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2515-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
Show the 25 most recent of 75 recalls
2010
- 30 Aug 2010 Z-2516-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2517-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2518-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2519-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2520-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2521-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2522-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2523-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2524-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2525-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2526-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2527-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2528-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2529-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
- 30 Aug 2010 Z-2530-2010 Unclassified (pre-2012) Terminated Huber needles may core and result in port leakage or emboli being flushed our of the port.
Frequently asked questions
How many devices does Multi-Med, Inc. have in the registry?
The registry currently lists 8 devices for Multi-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Multi-Med, Inc.'s devices?
Among its 8 most recently registered devices, Multi-Med, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Multi-Med, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Multi-Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Multi-Med, Inc.?
FDA recall records list 75 recalls initiated by Multi-Med, Inc., the most recent initiated on 30 Aug 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Multi-Med, Inc. in the registry?
The most recently registered devices listed for Multi-Med, Inc. include INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION), ENTERAL FEEDING CONTAINER, EXTERNAL FEEDING SET FOR PUMP USE and INTRAVASCULAR ADMINISTRATION SET.