HomeUSAGarrison Dental Solutions, LLC

Garrison Dental Solutions, LLC

USA · Spring Lake
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada — 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
10listed device types
Class I 9Class II 1Class III 0
plus 11 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
8registered devices
Class I 7Class II 1
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
1registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
1 including historic records
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 States11 registration records, 3 510(k), 0 PMA
Brazil8 confirmed, 0 excluded
Saudi Arabia1 confirmed, 0 excluded
Manufacturer names merged into this page: GARRISON DENTAL SOLUTIONS · GARRISON DENTAL SOLUTIONS LLC · Garrison Dental Solutions L.L.C.

Company information

Country
USA
City
Spring Lake

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

12009 · K091533
12020 · K200775
12024 · K241238

FDA listed device types

showing 8 of 10
Retainer, Matrix 1Instruments, Dental Hand 1Disk, Abrasive 1Wheel, Polishing Agent 1Forceps, Rubber Dam Clamp 1Instrument, Filling, Plastic, Dental 1Point, Abrasive 1Handle, Instrument, Dental 1

Registration details (sample)

MarketIdentifierNameClass / date
USK241238LOOP™ LED Curing Light System (CLK01)2024-08-01
USK200775LOOP LED Curing Light System2020-08-14
USK091533SLICKS SECTIONAL MATRIX AND MATRIX BANDS, MODELS SM100, SM150, SM175, SM200, SM300, SMH100, SMH150, SMH175 AND SMH2002009-08-17
BR10336460050MATRIZ SECCIONAL ORALTECHClass II
BR10336460115WEDGE WANDSClass I
BR10336460085COMPOSI-TIGHT 3D SECTIONAL MATRIX SYSTEMClass I
SAME0000019038SFDAA00001Composi Tight ® 3D Fussion ™ Sectional Matrix System

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