FDA.reportPublic FDA data

Medtimo, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30135086473013508647Medtimo, Inc.1Y2026-01-017625 Golden Triangle Dr Ste G Eden Prairie MN US 55344

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2067451160669587P160001OBALON BALLOON SYSTEMLTI2016-09-08
2067451978019213P130019MAESTRO RECHARGEABLE SYSTEMPIM2015-01-14
2067451250505105P000008LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEMLTI2001-06-05
2067451662269577K241039ReShape Calibration Tubes (B-2032, B-2036, B-2040); ReShape Calibration Tubes (B-2017); Gastric Balloon Suction Catheter (B-2020)KNT2024-05-16
2067451985148714K230131ReShape Calibration TubesKNT2023-02-15
2067451569552643K221898Gastrointestinal Boundary Identifier (GIBI HD)KNT2022-07-28
2067452067464875K220455Lap-Band System Calibration TubeKNT2022-06-07
2067451583112105K130424STIMEL-03IPF2013-07-11
2067451301257265K002838GASTRIC SUCTION AND DRAINAGE CATHETERKNT2001-07-09
2067451595920141

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KNT62024-05-16
LTI32016-09-08
PIM12015-01-14
IPF12013-07-11