Data / Medical devices / United States / PMT Corp.
PMT Corp.: FDA-registered device maker in Chanhassen, MN, United States, 19 510(k) clearances
PMT Corp. is registered with the FDA (registration 2182979) in Chanhassen, MN, United States. It lists 20 device types. The FDA files 19 510(k) clearances under its listings, the newest dated September 30, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2182979
- Address
- 1500 Park RD, Chanhassen, MN, United States, 55317
- Owner or operator
- PMT CORP. (2182979)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer
- First device listed
- August 1, 1983
- Registered through
- 2026
- Brand names listed
- ACCUSPAN, AFT Cannulas, Alura, Alura Vaginal Stent, Anchor Bolt, CABLE, CERVMAX, CORTAC and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Cable, Electrode | IKD | 2 | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Catheter And Tip, Suction | JOL | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Drape, Surgical, Antimicrobial | KKX | 2 | Manufacturer | accessdata.fda.gov |
| Electrode, Cortical | GYC | 2 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Electrode, Depth | GZL | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Instrument, Microsurgical | GZX | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Instrument, Surgical, Non-Powered | HAO | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Marker, Colon | NBG | 2 | Manufacturer | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Specification developer | accessdata.fda.gov |
| Neurological Stereotaxic Instrument | HAW | 2 | Manufacturer | accessdata.fda.gov |
| Orthosis, Cervical | IQK | 1 | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Orthosis, Truncal/Orthosis, Limb | MRI | 1 | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Pad, Kelly | FNW | 2 | Manufacturer | accessdata.fda.gov |
| Probe, Radiofrequency Lesion | GXI | 2 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Stent, Vaginal | KXP | 2 | Manufacturer | accessdata.fda.gov |
| Tissue Expander And Accessories | LCJ | U | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Tong, Skull For Traction | HAX | 2 | Manufacturer, Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 30, 2020 | K202542 | Allura Vaginal Stent | KXP | Substantially Equivalent | Pmt Corporation | accessdata.fda.gov |
| July 14, 2016 | K151790 | PMT Platinum Depthalon Depth Electrode | GZL | Substantially Equivalent | Pmt Corporation | accessdata.fda.gov |
| July 28, 2009 | K090733 | PMT HALO SYSTEM | HAX | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| May 8, 2009 | K082474 | PMT SUBDURAL CORTICAL ELECTRODES | GYC | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| March 16, 2005 | K042901 | ENDOMARK STERILE INDIA INK | NBG | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| August 3, 2004 | K033730 | PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIES | GZL | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| April 29, 1997 | K970418 | PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) | GZL | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| March 19, 1997 | K964224 | STAINLESS STEEL CORTAC CORTICAL ELECTRODE(2111)/PLANTINUM CORTAC CORTICAL ELECTRODE | GYC | Substantially Equivalent | Pmt Corp. | accessdata.fda.gov |
| June 19, 1987 | K871663 | PMT TRACTION TONGS | HAX | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| July 30, 1985 | K845035 | ELECTRODE FOR NEUROLOGICAL SURGERY 2111 | GYC | Substantially Equivalent for Some Indications | Progress Mankind Technology | accessdata.fda.gov |
| June 26, 1985 | K845036 | TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 | LCJ | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| May 30, 1984 | K831117 | MICROMAT W/VARIOUS MODELS | FNW | Substantially Equivalent | Pmt, Inc. | accessdata.fda.gov |
| February 17, 1984 | K834047 | PMT-HALO/ORTHOPEDIC JACKET SYSTEM | HAX | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| June 15, 1983 | K831329 | PMT VAXIOM STEREOTACTIC SYS #FX001 | HAW | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| November 19, 1980 | K802152 | PMT DEPTHALON DEPTH #2102 | GZL | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| November 19, 1980 | K802151 | PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC | GZL | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| November 12, 1980 | K802243 | VAXIOM FAMILY OF RF LESION PROBES & ELEC | GXI | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| May 30, 1980 | K801134 | MICROVAC | JOL | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
| May 30, 1980 | K801127 | MACROVAC | JOL | Substantially Equivalent | Progress Mankind Technology | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter And Tip, Suction
- All makers of Tong, Skull For Traction
- All makers of Needle, Aspiration And Injection, Disposable
- All makers of Electrode, Depth
- All makers of Tissue Expander And Accessories
- All makers of Instrument, Microsurgical
Updated September 30, 2020. 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.