# Ortho Technology, Inc.

- Location (FDA's records): Tampa, FL
- FDA decisions: 4 (2000–2012): 4 510(k) clearances
- Names in FDA's records: Ortho Technology, Inc. (2); Ortho Technology (2)
- Product codes: NJM (2), DZB (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- World Bio Tech Co., Ltd.: 1 (https://510kreport.com/company/world-bio-tech)
- Ht Co., Ltd.: 1 (https://510kreport.com/company/ht)
- Star Dentech Korea., Corp: 1 (https://510kreport.com/company/star-dentech-korea)
- Koroad America: 1 (https://510kreport.com/company/koroad-america)
- Speed Dental Co., Ltd.: 1 (https://510kreport.com/company/speed-dental)
- Biomers Products, LLC: 1 (https://510kreport.com/company/biomers-products)
- Orthosun Co., Ltd.: 1 (https://510kreport.com/company/orthosun)
- Sawbros Industries Pvt., Ltd.: 1 (https://510kreport.com/company/sawbros-industries-pvt)

## Its most-cited devices
- K073045: Sapphire Ceramic Bracket (2007), cited by 7
- K000358: Multi Adjustable Face Mask (2000), cited by 1

## Recent decisions
- K112707: Generation C Aesthetic Self-Ligating Bracket System (Jan 13, 2012)
- K073045: Sapphire Ceramic Bracket (Dec 18, 2007)
- K051751: Equa-Pull Safety Release Module (Jul 22, 2005)
- K000358: Multi Adjustable Face Mask (Jun 9, 2000)

Source page: https://510kreport.com/company/ortho-technology