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aap Implantate AG

Germany · Berlin · www.aap.de

✓ Record-verifiedregistrations found in 9 marketsEU SRN DE-MF-000005994

This company has registrations in European Union, United States, Brazil, Saudi Arabia, Taiwan, South Korea, Australia, Israel, Russia — 9 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

278UDI-DI device records

Class I 200Class IIb 78

USUnited StatesFDA openFDA

24listed device types

Class I 18Class II 6Class III 0

plus 53 registration records and 37 510(k)

UKUnited KingdomMHRA PARD

0registered device records

BRBrazilANVISA

8registered devices

Class I 8

22 including historic records

SASaudi ArabiaSFDA

46registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

TWTaiwanTFDA

3valid device licences

Class I 1Class II 2

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

1GMP quality-system certificates

Import 1

AUAustraliaTGA ARTG

2active ARTG entries

IIa 2

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

1registrations

RURussiaRoszdravnadzor

1active registrations

Class 3 1

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.

European Union278 raw hits, 0 excluded, 278 confirmed

United States53 registration records, 37 510(k), 0 PMA, 1 excluded

United Kingdom0 confirmed, 1 excluded

Brazil8 confirmed, 1 excluded

Saudi Arabia46 confirmed, 0 excluded

Manufacturer names merged into this page: AAP IMPLANTATE AG · aap Implantate AG

Regulatory identity

EU manufacturer SRN: DE-MF-000005994

Business registration

LEI: 39120001TRQTQ01LPP41
Registered address: Lorenzweg 5, Berlin, 12099
Registry record updated: 2023-11-16

Business registration data from GLEIF, retrieved 2026-09-02. Public registry information only; details of directors and shareholders are not collected.

FDA 510(k) clearances by year

11999

22002

12003

12004

12007

22008

12011

62012

62013

42014

12015

42016

22019

22021

12023

12024

12026

FDA listed device types

showing 8 of 24

Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component 1Pin, Fixation, Smooth 1Plate, Fixation, Bone 1Screw, Fixation, Bone 1Pin, Fixation, Threaded 1Washer, Bolt Nut 1Instrument, Bending Or Contouring 1Screwdriver 1

Registration details (sample)

Market	Identifier	Name	Class / date
EU	04042409385759	LOQTEQ®	Class IIb
EU	04042409385704	LOQTEQ®	Class IIb
EU	04042409385667	LOQTEQ®	Class IIb
EU	04042409355134	LOQTEQ®	Class IIb
US	K254253	LOQTEQ® VA Proximal Humerus Plate 3.5	2026-03-24
US	K233008	Cannulated Headless Bone Screws	2024-06-05
US	K230141	LOQTEQ® VA Elbow Plates 2.7/3.5 System	2023-03-17
BR	10242780123	Conjunto de instrumental para Punho LOQTEQ	Class I
BR	10242780061	KIT DE INSTRUMENTAL AAP	Class I
BR	10242780076	KIT DE INSTRUMENTAL PARA IMPLANTES AAP	Class I
SA	ME0000006423SFDAA00084	iming arm LOQTEQ® Distal Medial Humerus Plate	—
SA	ME0000006423SFDAA00120	Screwdriver	—