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LifeNet Health

USA · Virginia Beach
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Taiwan, Israel — 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
11listed device types
Class I 1Class II 9Class III 1
plus 27 registration records and 3 510(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
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
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 States27 registration records, 3 510(k), 0 PMA, 1 excluded
Manufacturer names merged into this page: LifeNet Health · LifeNet Health Northwest · LIFENET HEALTH
Same-named companies — This database also contains companies with near-identical names: LifeNet Health Northwest. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA
City
Virginia 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

12008 · K081438
12020 · K201338
12024 · K242799

FDA listed device types

showing 8 of 11
Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon 1Filler, Bone Void, Calcium Compound 1Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 1Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 1Fastener, Fixation, Biodegradable, Soft Tissue 1Suture, Nonabsorbable, Synthetic, Polyethylene 1Syringe, Piston 1Screw, Fixation, Bone 1

Registration details (sample)

MarketIdentifierNameClass / date
USK242799PliaFX Flo2024-11-21
USK201338Allograft MIS Delivery System2020-07-13
USK081438MATRACELL DECELLULARIZED PULMONARY ARTERY PATCH ALLOGRAFT2008-10-17

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