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Home›GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDA

GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDA

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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
6listed device types
Class I 0Class II 5Class III 0unclassified 1
plus 17 registration records and 43 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
25 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
7 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 States17 registration records, 43 510(k), 0 PMA, 2 excluded
Manufacturer names merged into this page: GEISTLICH PHARMA AG · GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDA
Same-named companies — This database also contains companies with near-identical names: GEISTLICH PHARMA AG. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

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

11988
11992
31995
11997
31998
12000
12002
12004
22011
12012
12013
12014
32017
12018
22019
22021
22022
22024
72025
32026

FDA listed device types

Filler, Bone Void, Calcium Compound 1Bone Grafting Material, Animal Source 1Barrier, Animal Source, Intraoral 1Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon 1Mesh, Surgical 1Wound Dressing With Animal-Derived Material(S) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK260364Device 300419 Strip2026-06-02
USK260532Derma-Gide2026-03-19
USK251323Device 104 Particulate2026-01-22

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