HomeUSAThe Emerging Technologies Group

The Emerging Technologies Group

USA · N. Palm Beach
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Australia, Hong Kong — 4 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
5listed device types
Class I 3Class II 2Class III 0
plus 9 registration records and 12 510(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
5 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
21active ARTG entries
Class I 20IIb 1
HKHong KongMDACS
1valid listings
Class III 1
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 States9 registration records, 12 510(k), 0 PMA
Manufacturer names merged into this page: JACOBS EMERGING TECHNOLOGIES, LLC · EIT EMERGING IMPLANT TECHNOLOGIES GMBH

Company information

Country
USA
City
N. Palm Beach

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

61996 · K961385
11997 · K961381
22017 · K172888
12018 · K181644
12019 · K183447
12020 · K201605

FDA listed device types

Orthopedic Manual Surgical Instrument 1Instruments, Surgical, Cardiovascular 1Tray, Surgical, Instrument 1Intervertebral Fusion Device With Bone Graft, Lumbar 1Intervertebral Fusion Device With Bone Graft, Cervical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK201605EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium ALIF Cage, EIT Cellular Titanium TLIF Cage, EIT Cellular Titanium LLIF Cage, EIT Cellular Titanium T/PLIF Cage2020-07-15
USK183447EIT Cellular Titanium Lumbar Cage - T/PLIF2019-02-04
USK181644EIT Cellular Titanium® Lumbar Cage LLIF2018-10-12

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