HomeUSAEAGLE LABS, LLC

EAGLE LABS, LLC

USA · Rancho Cucamonga
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Australia — 5 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
6listed device types
Class I 3Class II 3Class III 0
plus 6 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
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
4active device licences
Class II 4
8 including historic records
TWTaiwanTFDA
3valid device licences
Class I 3
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States6 registration records, 0 510(k), 0 PMA, 25 excluded
Brazil2 confirmed, 3 excluded
Saudi Arabia0 confirmed, 3 excluded
Canada4 confirmed, 2 excluded
Manufacturer names merged into this page: EAGLE LABS, LLC · EAGLE LABS LLC.

Company information

Country
USA
City
Rancho Cucamonga

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 listed device types

Sponge, Ophthalmic 1Lens, Contact, Polymethylmethacrylate, Diagnostic 1Needle, Conduction, Anesthetic (W/Wo Introducer) 1Cannula, Ophthalmic 1Knife, Ophthalmic 1Device, Irrigation, Ocular Surgery 1

Registration details (sample)

MarketIdentifierNameClass / date
BR80420200079VISION LINE PVA SPEARSClass II
BR80420200078VISION LINE CELLULOSE SPEARSClass II
CA73114EENT SINGLE-USE SURGICAL BLADESClass II
CA74727OPHTHALMIC LIGHT SHIELDSClass II
CA74729CORNEAL MARKING PADSClass II

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