HomeUSACompression Works, Inc.

Compression Works, Inc.

USA · Birmingham
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Australia, Israel — 4 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
1listed device types
Class I 0Class II 1Class III 0
plus 1 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class I 1
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States1 registration records, 3 510(k), 0 PMA, 11 excluded
Brazil1 confirmed, 1 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: COMPRESSION WORKS INC.

Company information

Country
USA
City
Birmingham

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12011 · K112384
12013 · K133029
12023 · K221661

FDA listed device types

Clamp, Vascular 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221661Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)2023-03-03
USK133029ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE2013-12-06
USK112384ABDOMINAL TOURNIQUET SYSTEM2011-10-18
BR80565170018AAJT-S (Abdominal Aortic & Junctional Tourniquet–Stabilized)Class I

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