FDA.reportPublic FDA data

PEDICRAFT, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
10435681043568PEDICRAFT, INC.1N2026-01-014134 ST. AUGUSTINE RD. P.O. BOX 5969 JACKSONVILLE FL US 32247

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
00766923025215Pedi Board - Pedi Board 1x3904-396-9627info@pedicraft.com
00766923025222Pedi Board - Pedi Board 1x4904-396-9627info@pedicraft.com
00766923025239Pedi Board - Pedi Board 2x4904-396-9627info@pedicraft.com
00766923025246Pedi Board - Pedi Board 2x6904-396-9627info@pedicraft.com
00766923025253Pedi Board - Pedi Board 3x8904-396-9627info@pedicraft.com
00766923025260Pedi Board - Pedi Board 3x15904-396-9627info@pedicraft.com
00766923348109Stay Safe Bed - Stay Safe Bed HE904-396-9627info@pedicraft.com
00766923348123Stay Safe - Stay Safe Bed HE HA9043969627info@pedicraft.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
6051658927620K905630INFANT REFLUX SLINGFRP1991-03-13
6051868391137K905629PEDICRAFT INFANT REFLUX WEDGEFRP1991-03-13
6051414364256
6051022159288
6051575237167
6051792706466
6051984591178

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FRP21991-03-13

PMN#

GUDID#

44 records. Showing 1-40. Next