| Primary Device ID | B095302123 |
| NIH Device Record Key | ec7400d6-3fb3-405b-9eb6-07b2ff77d2bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hintermann Series H3 |
| Version Model Number | 1 |
| Catalog Number | 302123 |
| Company DUNS | 080101891 |
| Company Name | Dt Medtech, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com | |
| Phone | 800-521-5002 |
| quality@dtmedtech.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B095302123 [Primary] |
| NTG | Prosthesis, Ankle, Uncemented, Non-Constrained |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2025-09-05 |
| Device Publish Date | 2019-08-19 |
| B0953302206 | H3 TIBIAL COMPONENT LEFT SIZE 6 |
| B0953302205 | H3 TIBIAL COMPONENT LEFT SIZE 5 |
| B0953302204 | H3 TIBIAL COMPONENT LEFT SIZE 4 |
| B0953302203 | H3 TIBIAL COMPONENT LEFT SIZE 3 |
| B0953302202 | H3 TIBIAL COMPONENT LEFT SIZE 2 |
| B0953302201 | H3 TIBIAL COMPONENT LEFT SIZE 1 |
| B0953302125 | FC TALAR COMPONENT LEFT SIZE 5 |
| B0953302124 | FC TALAR COMPONENT LEFT SIZE 4 |
| B0953302123 | FC TALAR COMPONENT LEFT SIZE 3 |
| B0953302122 | FC TALAR COMPONENT LEFT SIZE 2 |
| B0953302121 | FC TALAR COMPONENT LEFT SIZE 1 |
| B0953302116 | TALAR COMPONENT LEFT SIZE 6 |
| B0953302115 | TALAR COMPONENT LEFT SIZE 5 |
| B0953302114 | TALAR COMPONENT LEFT SIZE 4 |
| B0953302113 | TALAR COMPONENT LEFT SIZE 3 |
| B0953302112 | TALAR COMPONENT LEFT SIZE 2 |
| B0953302111 | TALAR COMPONENT LEFT SIZE 1 |
| B0953301125 | FC TALAR COMPONENT RIGHT SIZE 5 |
| B0953301124 | FC TALAR COMPONENT RIGHT SIZE 4 |
| B0953301123 | FC TALAR COMPONENT RIGHT SIZE 3 |
| B0953301122 | FC TALAR COMPONENT RIGHT SIZE 2 |
| B0953301121 | FC TALAR COMPONENT RIGHT SIZE 1 |
| B0953301116 | TALAR COMPONENT RIGHT SIZE 6 |
| B0953301115 | TALAR COMPONENT RIGHT SIZE 5 |
| B0953301114 | TALAR COMPONENT RIGHT SIZE 4 |
| B0953301113 | TALAR COMPONENT RIGHT SIZE 3 |
| B0953301112 | TALAR COMPONENT RIGHT SIZE 2 |
| B0953301111 | TALAR COMPONENT RIGHT SIZE 1 |
| B0953300609 | H3 PE INLAY SIZE 6- 9mm |
| B0953300607 | H3 PE INLAY SIZE 6- 7mm |
| B0953300606 | H3 PE INLAY SIZE 6- 6mm |
| B0953300605 | H3 PE INLAY SIZE 6- 5mm |
| B0953300509 | H3 PE INLAY SIZE 5- 9mm |
| B0953300507 | H3 PE INLAY SIZE 5- 7mm |
| B0953300506 | H3 PE INLAY SIZE 5- 6mm |
| B0953300505 | H3 PE INLAY SIZE 5- 5mm |
| B0953300409 | H3 PE INLAY SIZE 4- 9mm |
| B0953300407 | H3 PE INLAY SIZE 4- 7mm |
| B0953300406 | H3 PE INLAY SIZE 4 - 6 mm |
| B0953300405 | H3 PE INLAY SIZE 4- 5mm |
| B0953300309 | H3 PE INLAY SIZE 3- 9mm |
| B0953300307 | H3 PE INLAY SIZE 3 - 7mm |
| B0953300306 | H3 PE INLAY SIZE 3 - 6mm |
| B0953300305 | H3 PE INLAY SIZE 3 - 5mm |
| B0953300209 | H3 PE INLAY SIZE 2 - 9mm |
| B0953300207 | H3 PE INLAY SIZE 2 - 7mm |
| B0953300206 | H3 PE INLAY SIZE 2 - 6mm |
| B0953300205 | H3 PE INLAY SIZE 2 - 5mm |
| B0953300109 | H3 PE INLAY SIZE 1 - 9mm |
| B0953300107 | H3 PE INLAY SIZE 1 -7mm |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HINTERMANN SERIES H3 88378397 not registered Live/Pending |
DT MEDTECH, LLC. 2019-04-09 |
![]() HINTERMANN SERIES H3 86848313 not registered Dead/Abandoned |
DT MEDTECH, LLC 2015-12-14 |