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ALLUMIN8 INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30432349533043234953ALLUMIN8 INC1N2026-01-013158 W Lakefront Ct Springfield MO US 65810

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
00850062071902A8 INTEGR8® Porous Pedicle Screw System - Ti Rod - Straight 6.0x80mm+1 (417) 689-2424info@allumin8.com
00850080771846A8 INTEGR8® Porous Pedicle Screw System - Ti Rod - Lordosed 5.5x130mm+1 (417) 689-2424info@allumin8.com
00850080771853A8 INTEGR8® Porous Pedicle Screw System - Ti Rod - Lordosed 5.5x140mm+1 (417) 689-2424info@allumin8.com
00850080771860A8 INTEGR8® Porous Pedicle Screw System - Ti Rod - Lordosed 5.5x150mm+1 (417) 689-2424info@allumin8.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3480411476820287K242827A8 INTEGR8™ Porous Pedicle ScrewsNKB2025-10-20

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NKB12025-10-20

PMN#

GUDID#

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