# Gm Dos Reis Industria E Comerico Ltda.

- Location (FDA's records): Campinas, BR
- FDA decisions: 3 (2019–2023): 3 510(k) clearances
- Product codes: MBI (1), NKB (1), HRS (1)
- 510(k) review time since 2016: median 329 days, against 84 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 5 (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 whose devices it cites most
- Medartis AG: 2 (https://510kreport.com/company/medartis)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Neoortho Productos Orthopedicos S/A: 1 (https://510kreport.com/company/neoortho-productos-orthopedicos-s-a)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)

## Firms that cite its devices most
- GM Dos Reis Industria e Comercio Ltda.: 4 (https://510kreport.com/company/gm-dos-reis-industria-e-comercio)
- Ortobio S.A.: 1 (https://510kreport.com/company/ortobio)

## Its most-cited devices
- K182718: Mini and Micro Fragments Reconstruction System – GMReis (2019), cited by 4
- K223114: Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors (2023), cited by 1

## Recent decisions
- K223114: Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors (Aug 2, 2023)
- K182718: Mini and Micro Fragments Reconstruction System – GMReis (Dec 23, 2019)
- K180626: Pedimax II - Pedicular Screw Spinal System (Feb 1, 2019)

Source page: https://510kreport.com/company/gm-dos-reis-industria-e-comerico