FDA.reportPublic FDA data

PAN MEDICAL U.S. CORP.

Matched from indexed company URL: Pan Medical Ltd.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30111934693011193469PAN MEDICAL U.S. CORP.1Y2020-04-25Omni Business Park, Building V - Suite 505 7401 114th Avenue N Largo FL US 33773

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
15056033811252InterV Flex Catheter - 11 Gauge 15mm Balloon Kyphoplasty Flex Catheter (Mini)(727) 914-3932PanMed@PanMed.US
15060270904295InterV Flex Catheter - 11 Gauge 20mm Balloon Kyphoplasty Flex Catheter (Mini)(727) 914-3932PanMed@PanMed.US
15060270907937InterV-Curve Plus - 13 Gauge 15mm Balloon Kyphoplasty Long Catheter (Micro)(727) 914-3932PanMed@PanMed.US
15060270907944InterV-Curve Plus - 13 Gauge 20mm Balloon Kyphoplasty Long Catheter (Micro)(727) 914-3932PanMed@PanMed.US
15060270908880InterV - 11 Gauge 10mm Balloon Kyphoplasty Catheter (Mini)(727) 914-3932PanMed@PanMed.US
15060270908897InterV - 11 Gauge 15mm Balloon Kyphoplasty Catheter (Mini)(727) 914-3932PanMed@PanMed.US
15060270908903InterV - 11 Gauge 20mm Balloon Kyphoplasty Catheter (Mini)(727) 914-3932PanMed@PanMed.US

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2259432057838547K16245313G InterV Kyphoplasty Catheter (Micro) and 11G InterV Kyphoplasty Catheter (Mini-Flex)NDN2016-11-01
2259431168599510K150322InterV Kyphoplasty Catheter (Balloon Length: 10,15 and 20mm) InterV Kyphoplasty Catheter (Mini) (Balloon Length: 10, 15 and 20mm)NDN2015-03-06
2259431742085760K132620INTER V KYPHOPLASTY CATHETER (BALLOON LENGTH: 0 MM), INTERV KYPHOPLASTY CATHETER (BALLOON LENGHT: 15 MM), INTERV KYPHOPLNDN2014-04-16
2259431318199175
2259431614221973

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NDN32016-11-01

PMN#

GUDID#