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PROGRESSIVE MEDICAL, INC.

US

Last updated May 24, 2026

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
3149615786
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
192135242

Catalogue (148)

Page 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Pmi PMITCSG
FDA UDI
Class IActive
Pmi PMIS2215
FDA UDI
Class IIActive
Pmi PMICC512S
FDA UDI
Class IActive
Pmi P1652
FDA UDI
Class IIActive
Pmi PMI191YES
FDA UDI
Class IIActive
Pmi P0012AM
FDA UDI
Class IIActive
Pmi P0016M
FDA UDI
Class IIActive
Pmi PMI9111
FDA UDI
Class IIActive
Pmi P0118A
FDA UDI
Class IIActive
Pmi P0440
FDA UDI
Class IIActive
Pmi K703
FDA UDI
N/AActive
Pmi P1652
FDA UDI
Class IIActive
Pmi PMI205S
FDA UDI
Class IIActive
Pmi PMI203YES
FDA UDI
Class IIActive
Pmi PMIORCAP20
FDA UDI
Class IUnknown
Pmi P0013
FDA UDI
Class IIActive
Pmi PMIS2015
FDA UDI
Class IIActive
Pmi PMI150ML
FDA UDI
Class IIActive
Pmi P0022S
FDA UDI
Class IIActive
Pmi PMI250ML
FDA UDI
Class IIActive
Pmi P0017
FDA UDI
Class IIActive
Pmi K411C
FDA UDI
N/AActive
Pmi P0020S
FDA UDI
Class IIActive
Pmi PMIPIN15
FDA UDI
Class IIActive
Pmi P0027S
FDA UDI
Class IIActive
Pmi P0028M
FDA UDI
Class IIActive
Pmi PMIIN12
FDA UDI
Class IIUnknown
Pmi PMIXLPIN
FDA UDI
Class IUnknown
Pmi P1650
FDA UDI
Class IIActive
Pmi PMIS2023
FDA UDI
Class IIActive
Pmi P0020X
FDA UDI
Class IIActive
Pmi PMIORCAP20
FDA UDI
Class IIActive
Pmi P0113
FDA UDI
Class IIActive
Pmi P0012M
FDA UDI
Class IIActive
Pmi P0490
FDA UDI
Class IIActive
Pmi P0410
FDA UDI
Class IIActive
Pmi PMIXL11
FDA UDI
Class IActive
Pmi P0014
FDA UDI
Class IIActive
Pmi P0014A
FDA UDI
Class IIActive
Pmi P0100X
FDA UDI
Class IIActive
Pmi PMITCSGXL
FDA UDI
Class IActive
Pmi P0028
FDA UDI
Class IIActive
Pmi PMI221S
FDA UDI
Class IIActive
Pmi PMIX02
FDA UDI
Class IIActive
Pmi PMI-1522
FDA UDI
Class IActive
Pmi P0020SX
FDA UDI
Class IIActive
Pmi PMI500ML
FDA UDI
Class IIActive
Pmi PMI790-001
FDA UDI
Class IIActive
Pmi PMIORCB
FDA UDI
Class IActive
Pmi PMIORCA
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.

DateRecall No.ClassStatusReason
Apr 12, 2013Z-1351-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1356-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1355-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1350-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1354-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1358-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1357-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1364-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1352-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1348-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1359-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1361-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1360-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1349-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1362-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1363-2013—terminated

Product coatings require 510K approval.

Apr 12, 2013Z-1353-2013—terminated

Product coatings require 510K approval.

Dec 9, 2011Z-0276-2013—terminated

Some of the sterile packages had broken seals.

Oct 28, 2011Z-0159-2013—terminated

The tip of the product could come loose or unravel.

Jul 28, 2011Z-0081-2012—terminated

The product may have a higher flow rate than specified resulting in over administration of drug solutions to the patients.