HomeUSAHill Laboratories Co.

Hill Laboratories Co.

USA · Frazer
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Taiwan, Singapore, Russia — 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
9listed device types
Class I 3Class II 5Class III 0unclassified 1
plus 17 registration records and 17 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
1 including historic records
TWTaiwanTFDA
1valid device licences
Class I 1
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2a 1
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 States17 registration records, 17 510(k), 0 PMA, 22 excluded
Brazil0 confirmed, 8 excluded
Saudi Arabia0 confirmed, 5 excluded
Canada0 confirmed, 4 excluded
Manufacturer names merged into this page: Hill Laboratories · HILL LABORATORIES

Company information

Country
USA
City
Frazer

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

11993
101995
12004
12006
12007
12008
12009
12010

FDA listed device types

showing 8 of 9
Apparatus, Traction, Non-Powered 1Table, Powered 1Exerciser, Powered 1Lamp, Infrared, Therapeutic Heating 1Equipment, Traction, Powered 1Table, Physical Therapy, Multi Function 1Interferential Current Therapy 1Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat 1

Registration details (sample)

MarketIdentifierNameClass / date
USK090250ELECTRO-LIGHT THERAPY2010-02-11
USK083183AKLARUS PHOTOTHERAPY SYSTEM2009-07-16
USK072256HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL2008-03-12

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