Data / Medical devices / United States / Multi-Med, Inc.
Multi-Med, Inc.: FDA-registered device maker in Keene, NH, United States, 25 510(k) clearances
Multi-Med, Inc. is registered with the FDA (registration 1221765) in Keene, NH, United States. It lists 7 device types. The FDA files 25 510(k) clearances under its listings, the newest dated December 14, 2017. 2 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1221765
- Address
- 26 Victoria Ct, Keene, NH, United States, 03431
- Owner or operator
- MULTI-MED, INC. (1221765)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- January 16, 2008
- Registered through
- 2026
- Brand names listed
- ISP Safety Huber Needle Infusion Set, NDSN-BL, NDSN-BU, NDSN-PK, NDSN-PU, NDSP-BL, NDSP-BU, NDSP-PK and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Urethral | GBM | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Non-Coring (Huber) Needle | PTI | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Feeding | FPD | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 14, 2017 | K170881 | ISP Safety Huber Needle Infusion Set | PTI | Substantially Equivalent | Infusion Safety Products, Inc. | accessdata.fda.gov |
| July 6, 2012 | K120195 | SAFETY SUBCUTANEOUS TISSUE INFUSION SET | FPA | Substantially Equivalent | Multi Med | accessdata.fda.gov |
| May 20, 2010 | K092628 | ENTERAL FEEDING TUBE AND ACCESSORIES, FEEDING TUBE EXTENSION SET | KNT | Substantially Equivalent | Alan Reid | accessdata.fda.gov |
| December 23, 2008 | K082818 | SUBCUTANEOUS NEEDLE INFUSION SET | FPA | Substantially Equivalent | Marcal Medical, Inc. | accessdata.fda.gov |
| June 17, 2003 | K031409 | URINARY CATHETERS | GBM | Substantially Equivalent | Promedic, Inc. | accessdata.fda.gov |
| July 16, 2002 | K020005 | INFANT FEEDING TUBES | KNT | Substantially Equivalent | Promedic, Inc. | accessdata.fda.gov |
| August 27, 1997 | K972469 | SELFSHIELD HN SELF SHEATHING HYPODERMIC NEEDLE | FMI | Substantially Equivalent | Beech Medical Products, Inc. | accessdata.fda.gov |
| March 13, 1995 | K946082 | BEECH PRO LOK FIXED | FPA | Substantially Equivalent | Beech Medical Products, Inc. | accessdata.fda.gov |
| December 29, 1993 | K933852 | PRO-LOK EXTENSION SET | FPA | Substantially Equivalent | Beech Medical Products, Inc. | accessdata.fda.gov |
| December 29, 1993 | K933749 | BEECH VERSA LOK | FPA | Substantially Equivalent | Beech Medical Products, Inc. | accessdata.fda.gov |
| December 29, 1993 | K933732 | BEECH PROLOK | FPA | Substantially Equivalent | Beech Medical, Inc. | accessdata.fda.gov |
| September 3, 1993 | K930750 | DURHAM; ADM. SET-LUER LOCK W/.22 MICRON FILTER | FPA | Substantially Equivalent | Intl. Medical Consultants | accessdata.fda.gov |
| March 15, 1993 | K922469 | PRO-LOK EXTENSION SET(S) | FPA | Substantially Equivalent | Vlv Associates, Inc. | accessdata.fda.gov |
| October 3, 1990 | K904217 | PRO-LOK (TM) EXTENSION SETS | FPA | Substantially Equivalent | Vlv Associates, Inc. | accessdata.fda.gov |
| June 8, 1990 | K901081 | PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY | FPA | Substantially Equivalent | Vlv Associates, Inc. | accessdata.fda.gov |
| June 8, 1990 | K901046 | VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR | FPA | Substantially Equivalent | Vlv Associates, Inc. | accessdata.fda.gov |
| June 14, 1989 | K890424 | ENTERAL FEEDING CONTAINER | KNT | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| May 23, 1989 | K890396 | EXTERNAL FEEDING SET FOR PUMP USE | FPD | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| May 18, 1989 | K891176 | INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) | FPA | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| May 5, 1989 | K891919 | INTRAVASCULAR ADMINISTRATION SET | FMI | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| April 21, 1989 | K891072 | INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| March 31, 1989 | K890340 | INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| February 3, 1989 | K890127 | INTRAVASCULAR ADMINISTRATION SET | FMI | Substantially Equivalent | Multi-Med, Inc. | accessdata.fda.gov |
| April 28, 1983 | K831088 | MINI-VOL I.V. SET | FPA | Substantially Equivalent | Beech Medical, Inc. | accessdata.fda.gov |
| April 28, 1983 | K831087 | MINI-VOL EXTENSION SET | FPA | Substantially Equivalent | Beech Medical, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| August 30, 2010 | 56548 | Not yet classified | Terminated | All Med Medical 19ga x.50" Winged Administration Set w/Y Site Model # M195Y Reorder # 50-1912 | Huber needles may core and result in port leakage or emboli being flushed our of the port. | accessdata.fda.gov |
| May 26, 2010 | 55824 | Not yet classified | Terminated | 22ga x 1" Straight Huber Needle This product is a small gauge needle intended for single use hypodermic access to implanted ports. | FDA sample determined the needles to be coring. | accessdata.fda.gov |
Compare with other makers
- All makers of Set, Administration, Intravascular
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Tubes, Gastrointestinal (And Accessories)
- All makers of Tube, Feeding
- All makers of Non-Coring (Huber) Needle
- All makers of Catheter, Urethral
Updated December 14, 2017. 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.