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Creative Research and Mfg., Inc.

USA · Mchenry

✓ 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

10listed device types

Class I 1Class II 9Class III 0

plus 10 registration records and 2 510(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

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 States10 registration records, 2 510(k), 0 PMA, 38 excluded

Brazil0 confirmed, 7 excluded

Saudi Arabia0 confirmed, 1 excluded

Canada0 confirmed, 2 excluded

Manufacturer names merged into this page: Creative Foam Corporation dba MT. OLIVE MFG

Same-named companies — This database also contains companies with near-identical names: Creative Foam Corporation dba MT. OLIVE MFG. Company name alone cannot separate their registrations, so the figures below may include either.

FDA 510(k) clearances by year

11981 · K810248

11982 · K820070

FDA listed device types

showing 8 of 10

System, Network And Communication, Physiological Monitors 1Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) 1Monitor, Breathing Frequency 1Generator, Oxygen, Portable 1Ventilator, Continuous, Facility Use 1System, Thermal Regulating 1Oximeter 1Transmitters And Receivers, Physiological Signal, Radiofrequency 1

Market	Identifier	Name	Class / date
US	K820070	MSI STERNUM ASPIRATION NEEDLE	1982-02-04
US	K810248	MSI BONE MARROW BIOPSY NEEDLE W/J TIP	1981-03-20

Creative Research and Mfg., Inc.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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