HomeUSAHOLLYWOG, LLC

HOLLYWOG, LLC

USA · Chattanooga
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Singapore, Australia, Israel — 6 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
4listed device types
Class I 1Class II 3Class III 0
plus 3 registration records and 4 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class 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
4active device licences
Class II 4
6 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 1IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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 States3 registration records, 4 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Canada4 confirmed, 0 excluded
Manufacturer names merged into this page: HOLLYWOG, LLC · HOLLYWOG

Company information

Country
USA
City
Chattanooga

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

22012 · K120500
12015 · K150695
12017 · K171599

FDA listed device types

Equipment, Traction, Powered 1Stimulator, Nerve, Transcutaneous, Over-The-Counter 1Stimulator, Electrical, Transcutaneous, For Arthritis 1Massager, Therapeutic, Electric 1

Registration details (sample)

MarketIdentifierNameClass / date
USK171599WiTouch Pro, WiTouch, Neubac2017-09-22
USK150695Modpod2015-08-13
USK120500THE PAIN PILOT (A.K.A PAIN PILOT)2012-08-20
BR80130610007ELETRODO ADESIVOClass II
CA85366HOLLYWOG EMSClass II
CA85367HOLLYWOG TENSClass II
CA85883HOLLYWOG ELECTRODESClass II

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