HomeUSAR. Wolf Medical Instruments Corp.

R. Wolf Medical Instruments Corp.

USA · Walker
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
30listed device types
Class I 5Class II 25Class III 0
plus 36 registration records and 155 510(k), 4 PMA
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
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 States36 registration records, 155 510(k), 4 PMA, 11 excluded
Brazil0 confirmed, 5 excluded
Saudi Arabia0 confirmed, 6 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: RICHARD WOLF MEDICAL INSTRUMENTS CORP.

Company information

Country
USA
City
Walker

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

52000
92001
22002
52003
32004
32005
22007
22008
12009
22012
12013
12016
22017
12018
12019
12020
32021
12022
12023
12024

FDA listed device types

showing 8 of 30
Syringe, Irrigating (Non Dental) 1Scissors, Orthopedic, Surgical 1Accessories, Arthroscopic 1Accessories, Photographic, For Endoscope (Exclude Light Sources) 1Massager, Therapeutic, Electric 1Electrosurgical, Cutting & Coagulation & Accessories 1Cystoscope And Accessories, Flexible/Rigid 1Accessories, Cleaning, For Endoscope 1

Registration details (sample)

MarketIdentifierNameClass / date
USK231291Perforated Baskets2024-06-03
USK230194HF Surgery Generator 400KHZ2023-03-22
USK212808Logic Hd camera head green, System green2022-06-14

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