HomeGermanyHoogland Spine Products, GmbH

Hoogland Spine Products, GmbH

Germany · Munchen-Unterföhring
✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, Australia, Israel — 7 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
33listed device types
Class I 29Class II 4Class III 0
plus 36 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
5registered devices
Class I 1Class II 4
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
3 including historic records
TWTaiwanTFDA
3valid device licences
Class I 2Class II 1
SGSingaporeHSA SMDR
2device registrations
CLASS B 2
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
23active ARTG entries
Class I 19IIa 2IIb 2
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 States36 registration records, 3 510(k), 0 PMA
Brazil5 confirmed, 0 excluded
Manufacturer names merged into this page: Hoogland Spine Products GmbH · HOOGLAND SPINE PRODUCTS GMBH · HOOGLAND SPINE PRODUCTS GmbH.

Company information

Country
Germany

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

22009 · K083552
12022 · K211173

FDA listed device types

showing 8 of 33
Motor, Surgical Instrument, Ac-Powered 1Forceps 1Accessories, Cleaning Brushes, For Endoscope 1Probe 1Chisel, Surgical, Manual 1Scissors, Orthopedic, Surgical 1Punch, Surgical 1Guide, Surgical, Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
USK211173maxmorespine Bipolar Electrodes2022-06-23
USK083552MAXMORESPINE TOM STICK2009-10-09
USK090132MAXMORESPINE SPINAL SYSTEM2009-06-09
BR81504790308Instrumentos MaxmorespineClass I
BR81504799081Kit Canula para Drilagem de OssosClass II
BR81504799043Endoscópios Maxmorespine®Class II

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