DT MEDTECH LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30121047673012104767DT MEDTECH LLC1N2026-01-01111 Moffitt Street McMinnville TN US 37110

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
B095322315Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 5MM/ANTERIOR800-521-5002quality@dtmedtech.com
B095322316Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 6MM/ANTERIOR800-521-5002quality@dtmedtech.com
B095322317Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 7MM/ANTERIOR800-521-5002quality@dtmedtech.com
B095322325Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 5MM/POSTERIOR800-521-5002quality@dtmedtech.com
B095322326Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 6MM/POSTERIOR800-521-5002quality@dtmedtech.com
B095322327Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 7MM/POSTERIOR800-521-5002quality@dtmedtech.com
B095322329Hintermann Series H2 - H2 PE INLAY SIZE 3 LEFT 9MM/POSTERIOR800-521-5002quality@dtmedtech.com
B095329645Hintermann Series - T10 Driver Handle999-999-9999quality@dtmedtech.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2133611118640404P160036Hintermann Series H3 Total Ankle Replacement SystemNTG2019-06-04
2133611553630244K171004Hintermann Series H2 Total Ankle SystemHSN2017-11-07
2133611111121886
2133611181704189
2133611207798022
2133611405836848
2133611406568617
2133611529621265
2133611881650567
2133611892015382
2133611941863078
2133611963300095
2133611982931985
2133612038173445

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NTG12019-06-04
HSN12017-11-07

PMA#

PMN#

GUDID#

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