Primary Device ID | B15170907PA0 |
NIH Device Record Key | d4fbad08-e65a-4cf8-81d4-2b15c5af5eae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STARlight® PRO |
Version Model Number | 709.07PA |
Catalog Number | 709.07PA |
Company DUNS | 604405373 |
Company Name | ORTHOMERICA PRODUCTS, INC. |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
B15176507PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176407PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176307PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176207PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176107PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176007PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15170907PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15170407PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15170307PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |
B15176607PA0 | The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to imp |