Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
Pmi P0019S
FDA UDI
Class IIActive
Pmi P0113M
FDA UDI
Class IIActive
Pmi P0018S
FDA UDI
Class IIActive
Pmi P0026
FDA UDI
Class IIActive
Pmi PMITCSGXLKT
FDA UDI
Class IActive
Pmi PMISG12B2
FDA UDI
Class IActive
Pmi P0016
FDA UDI
Class IIActive
Pmi P0022
FDA UDI
Class IIActive
Pmi PMI191S
FDA UDI
Class IIActive
Pmi PMIFR200
FDA UDI
Class IIActive
Pmi P1653
FDA UDI
Class IIActive
Pmi K703C
FDA UDI
N/AActive
Pmi P0024S
FDA UDI
Class IIActive
Pmi PMICC512
FDA UDI
Class IActive
Pmi PMI201S
FDA UDI
Class IIActive
Pmi P0430
FDA UDI
Class IIActive
Pmi PMI-6000
FDA UDI
Class IActive
Pmi P0016AM
FDA UDI
Class IIActive
Pmi PMIFR100
FDA UDI
Class IIActive
Pmi K303
FDA UDI
N/AActive
Pmi PMI2015S
FDA UDI
Class IIActive
Pmi P0014M
FDA UDI
Class IIActive
Pmi P0100S
FDA UDI
Class IIActive
Pmi P0118
FDA UDI
Class IIActive
Pmi PMI512
FDA UDI
Class IActive
Pmi PMI100ML
FDA UDI
Class IIActive
Pmi PMI2215S
FDA UDI
Class IIActive
Pmi PMI2015YES
FDA UDI
Class IIActive
Pmi PMI2014S
FDA UDI
Class IIActive
Pmi PMI9222
FDA UDI
Class IIActive
Pmi PMISG10
FDA UDI
Class IActive
Pmi P0100
FDA UDI
Class IIActive
Pmi PMI50ML
FDA UDI
Class IIActive
Pmi P0018
FDA UDI
Class IIActive
Pmi P4500
FDA UDI
Class IIActive
Pmi PMI193S
FDA UDI
Class IIActive
Pmi PMI1915YES
FDA UDI
Class IIActive
Pmi PMIS2035
FDA UDI
Class IIActive
Pmi PMI201YES
FDA UDI
Class IIActive
Pmi P0035H
FDA UDI
Class IIActive
Pmi PMISG12B4
FDA UDI
Class IActive
Pmi P0012
FDA UDI
Class IIActive
Pmi P0016A
FDA UDI
Class IIActive
Pmi P0026S
FDA UDI
Class IIActive
Pmi PMI-10
FDA UDI
Class IActive
Pmi P0009
FDA UDI
Class IIActive
Pmi PMI1915S
FDA UDI
Class IIActive
Pmi PMILK40
FDA UDI
Class IActive
Pmi P0013M
FDA UDI
Class IIActive
Pmi PMI2215YES
FDA UDI
Class IIActive

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.