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Home›USA›LAP of America Laser Applications, LLC.

LAP of America Laser Applications, LLC.

USA · Boynton Beach
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 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
3listed device types
Class I 2Class II 1Class III 0
plus 7 registration records and 4 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class I 2Class II 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
pendingnot queried
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 States7 registration records, 4 510(k), 0 PMA, 6 excluded
Brazil3 confirmed, 1 excluded
Manufacturer names merged into this page: LAP of America Laser Applications, LLC. · LAP GMBH LASER APPLIKATIONEN

Company information

Country
USA
City
Boynton Beach

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

12018 · K173926
12020 · K200907
12024 · K232031
12026 · K253004

FDA listed device types

Monitor, Patient Position, Light-Beam 1Instrument, Quality-Assurance, Radiologic 1Accelerator, Linear, Medical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK253004LUNA 3D2026-06-04
USK232031LUNA 3D2024-03-29
USK200907Thales 3D Mr Scanner2020-06-03
BR81464750209DORADO/DORADOnovaClass I
BR81464750208DORADOnova MR3TClass I
BR80186820015DORADOSELECTClass II

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