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Gm Dos Reis Industria E Comercio

US

Last updated May 23, 2026

What Gm Dos Reis Industria E Comercio makes

Gm Dos Reis Industria E Comercio manufactures the Pectus Versa System, designed for surgical correction of pectus excavatum deformities, and the GMReis Fibula Nail System, used in orthopedic fixation for long bone fractures, particularly the tibia.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates within the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Gm Dos Reis Industria E Comercio manufacture?

Gm Dos Reis Industria E Comercio specializes in surgical devices for orthopedic and thoracic applications. Their portfolio includes the Pectus Versa System, which is intended for correcting pectus excavatum deformities (a sunken chest condition), and the GMReis Fibula Nail System, designed for internal fixation of long bone fractures, particularly in the tibia. These devices address distinct clinical needs in orthopedic and reconstructive surgery.

Where is Gm Dos Reis Industria E Comercio based, and what does that mean for its regulatory oversight?

The company is based in the United States, meaning its devices fall under FDA jurisdiction. Since the devices are classified as Class II, they require premarket notification (510(k)) clearance before commercial distribution. This classification reflects a moderate risk level, requiring evidence of substantial equivalence to a legally marketed predicate device.

Which regulatory registries or databases list Gm Dos Reis Industria E Comercio’s devices?

Gm Dos Reis Industria E Comercio’s devices are listed in the FDA’s 510(k) database, which tracks premarket notifications for Class II devices. This registry confirms the devices have undergone the required FDA review process for safety and effectiveness before entering the market. The listing serves as a public record of compliance with U.S. regulatory requirements.

How are Gm Dos Reis Industria E Comercio’s devices classified under FDA regulations, and why does this matter?

The company’s devices are classified as Class II under FDA regulations, indicating a moderate risk to patients. This classification requires manufacturers to demonstrate that their devices are substantially equivalent to a legally marketed predicate device through the 510(k) pathway. The classification ensures additional scrutiny beyond general controls (like manufacturing standards) but does not require the rigorous clinical trials associated with Class III devices, which pose higher risks.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (1723)

Page 9 of 35
DeviceModel / ReferenceRegistriesClassStatus
Cut Screw - Percutaneous Compression Screw Cut Screw - Sterile
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis VA Locking Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Hook Button Clavicle Plate Left 9.0mm 05 Holes 2.7mm
FDA UDI
Class IIActive
GMReis Fibula Nail System Locking Screw T10 Ø3,5mm X 22,0mm
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Locking Screw
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Fix-Max Zip Anchor
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Fix-Max Zip Anchor
FDA UDI
Class IIActive
GMReis Fibula Nail System Locking Screw T10 Ø3,5mm X 8,0mm
FDA UDI
Class IIActive
Versalock Rib and Sternum Plates System Versalock Rib and Sternum Screw–T7 Self Tapping Ø2.7 x 16.0mm
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini Cortical Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Superior Lateral Clavicle Plate with Anterior Tab Left 14 Holes 2.7/3.
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw - Sterile
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis WATERSHED DISTAL RADIUS VERSALOCK LOCKING PLATE 50.0MM X 26.0MM – WIDE – RIGHT
FDA UDI
Class IIActive
Versalock Rib and Sternum Plates System Versalock Rib and Sternum Screw–T7 Self Drilling Ø2.4 x 10.0mm
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Olecranon Versatile Plate Left 05 Holes 2.7/3.5 mm
FDA UDI
Class IIActive
GMReis Ankle Plating System ANATOMICAL FIBULA VERSALOCK PLATE RIGHT 11 HOLES - 2.7/3.5
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Superior Lateral Left Clavicle Plate 16 Holes 2.7/3.5mm
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini Cortical Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Superior Medial Medium Right Clavicle Plate 08 Holes 3.5mm
FDA UDI
Class IIActive
Pedimax II - Pedicular Screw Spinal System Monoaxial Pedicle Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw - Sterile
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Proximal Femur Plate
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSA TORXDRIVE SCREW LOW PROFILE Ø3.5X38MM T10
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Distal Femur Plate
FDA UDI
Class IIActive
Versalock Rib and Sternum Plates System Versalock Rib and Sternum Screw–T7 Self Drilling Ø2.4 x 18.0mm
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Zip Anchor
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Spacer Screw
FDA UDI
Class IIActive
GMReis Ankle Plating System ANATOMICAL MEDIAL TIBIA DISTAL VERSALOCK PLATE LEFT 04 HOLES 2.7/3.5MM
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Olecranon Versatile Plate Right 11 Holes 2.7/3.5 mm
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini Straight Plate
FDA UDI
Class IIActive
GMReis Ankle Plating System MINI CANNULATED COMPRESSION SCREW PARTIAL LONG THREAD Ø 4.0X13X26MM
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Pedimax II - Pedicular Screw Spinal System Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis VA Locking Screw
FDA UDI
Class IIActive
Orthopedic Instruments COUNTERSINK FOR SCREW 2.4 - 2.7MM
FDA UDI
Class IActive
Mini and Micro Fragments Reconstruction System - GMReis U Plate
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis FLP Plate
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Locking Screw
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK TORXDRIVE LOCKING SCREW LOW PROFILE Ø3.5X16MM T10
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Gm Dos Reis Industria E Comercio Ltda Campinas Sao Paulo · BR FEI 3013756169