FDA.reportPublic FDA data

PROVENT SLEEP THERAPY LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30116831223011683122PROVENT SLEEP THERAPY LLC1N2020-04-25125 Tolman Ave Leominster MA US 01453

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
00868020000208Provent Sleep Therapy - Provent 30 Night Standard Pack contains 30 Standard resistance Provent888-757-9355info@proventtherapy.com
00868020000215Provent Sleep Therapy - Provent 30 Night Starter Kit contains two (2) Light resistance (Phase 1) non-therapeutic acclimation units, two (2) Medium resistance (Phase 2) non-therapeutic acclimation units, and 26 Standard resistance Provent devices888-757-9355info@proventtherapy.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1840891795649123K102404PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50)OHP2010-12-02
1840891522455316K080983PROVENT NASAL CANNULAMNR2008-08-07

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OHP12010-12-02
MNR12008-08-07

GUDID#