LIVSMED

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30154171863015417186LIVSMED USA, INC.1Y2026-01-012305 Historic Decatur Road Suite 100 San Diego CA US 92106

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
08800042706111Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com
08800042706128Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com
08800042706135Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com
08800042706142Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com
08800042706159Artisential Monopolar Spatula - This device is a sterile, single-use instrument intended to be used with an electrosurgical generator to deliver electrosurgical current in a monopolar configuration for tissue incision and coagulation.8335487633infousa@livsmed.com
08809756910067Artisential Monopolar Spatula - This device is a sterile, single-use instrument intended to be used with an electrosurgical generator to deliver electrosurgical current in a monopolar configuration for tissue incision and coagulation.8335487633infousa@livsmed.com
08809756910081Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com
08809756910104Artisential Clip Applier Large - This device is a sterile, single-use instrument intended to ligate soft tissues and blood vessels.8335487633infousa@livsmed.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2274921075241013K190909ArtiSential Bipolar Fenestrated ForcepsGEI2020-02-13
2274922034304190K122560VERSALVENT MODEL V1 HYPERBARIC CHAMBER VENTILATOR MODEL V1CBK2013-03-26
2274921301163580
2274921575827844
2274921626732607

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI12020-02-13
CBK12013-03-26

PMN#

GUDID#

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