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Sign in to claim this brandPROGRESSIVE MEDICAL, INC.
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- progressivemedinc.com
- —
- —
- [email protected]
- Phone
- 3149615786
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 192135242
Catalogue (148)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pmi | P0021X | FDA UDI | Class II | Active |
| Pmi | P1651 | FDA UDI | Class II | Active |
| Pmi | PMI203S | FDA UDI | Class II | Active |
| Pmi | PMI-500 | FDA UDI | Class II | Active |
| Pmi | P0017S | FDA UDI | Class II | Active |
| Pmi | P0036H | FDA UDI | Class II | Active |
| Pmi | P0460 | FDA UDI | Class II | Active |
| Pmi | PMIXLPIN | FDA UDI | Class I | Active |
| Pmi | P0105S | FDA UDI | Class II | Active |
| Pmi | P0024 | FDA UDI | Class II | Active |
| Pmi | PMIFR300 | FDA UDI | Class II | Active |
| Pmi | P0420 | FDA UDI | Class II | Active |
| Pmi | P0450 | FDA UDI | Class II | Active |
| Pmi | PMI790-000 | FDA UDI | Class II | Active |
| Pmi | P0020 | FDA UDI | Class II | Active |
| Pmi | PMI1000ML | FDA UDI | Class II | Active |
| Pmi | PMIIN150 | FDA UDI | Class II | Active |
| Pmi | PMI154D | FDA UDI | Class I | Active |
| Pmi | P0012A | FDA UDI | Class II | Active |
| Pmi | PMI225S | FDA UDI | Class II | Active |
| Pmi | PMI-102 | FDA UDI | Class I | Active |
| Pmi | P0021 | FDA UDI | Class II | Active |
| Pmi | P0019 | FDA UDI | Class II | Active |
| Pmi | PMICATH20 | FDA UDI | Class I | Active |
| Pmi | PMI193YES | FDA UDI | Class II | Active |
| Pmi | PMIX03 | FDA UDI | Class II | Active |
| Pmi | P0015 | FDA UDI | Class II | Active |
| Pmi | P0105 | FDA UDI | Class II | Active |
| Pmi | P0021SX | FDA UDI | Class II | Active |
| Pmi | PMI223YES | FDA UDI | Class II | Active |
| Pmi | PMICCXLKT | FDA UDI | Class I | Active |
| Pmi | PMI223S | FDA UDI | Class II | Active |
| Pmi | P0014AM | FDA UDI | Class II | Active |
| Pmi | PMI1914S | FDA UDI | Class II | Active |
| Pmi | PMI790-SCREW | FDA UDI | Class II | Active |
| Pmi | P0480 | FDA UDI | Class II | Active |
| Pmi | P0470 | FDA UDI | Class II | Active |
| Pmi | PMILAP13 | FDA UDI | Class I | Active |
| Pmi | PMI12 | FDA UDI | Class I | Active |
| Pmi | PMIIN120 | FDA UDI | Class II | Active |
| Pmi | P0027 | FDA UDI | Class II | Active |
| Pmi | PMI221YES | FDA UDI | Class II | Active |
| Pmi | K705 | FDA UDI | N/A | Active |
| Pmi | PMIX01 | FDA UDI | Class II | Active |
| Pmi | PMIXTCR | FDA UDI | Class I | Active |
| Pmi | PMI9333 | FDA UDI | Class II | Active |
| Pmi | P0021S | FDA UDI | Class II | Active |
| Percutaneous Introducer Needle | K191295 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (20)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 12, 2013 | Z-1351-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1356-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1355-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1350-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1354-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1358-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1357-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1364-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1352-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1348-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1359-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1361-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1360-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1349-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1362-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1363-2013 | — | terminated | Product coatings require 510K approval. |
| Apr 12, 2013 | Z-1353-2013 | — | terminated | Product coatings require 510K approval. |
| Dec 9, 2011 | Z-0276-2013 | — | terminated | Some of the sterile packages had broken seals. |
| Oct 28, 2011 | Z-0159-2013 | — | terminated | The tip of the product could come loose or unravel. |
| Jul 28, 2011 | Z-0081-2012 | — | terminated | The product may have a higher flow rate than specified resulting in over administration of drug solutions to the patients. |