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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 30 of 35
DeviceModel / ReferenceRegistriesClassStatus
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini L Plate
FDA UDI
Class IIActive
Pedimax II - Pedicular Screw Spinal System Polyaxial Pedicle Screw
FDA UDI
Class IIActive
Pedimax II - Pedicular Screw Spinal System Rod to Rod Clamp
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Super Max Zip Anchor
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Superior Lateral Right Clavicle Plate 16 Holes 2.7/3.5mm
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Hook Clavicle Plate Right 12.0mm 11 Holes 2.7/3.5mm
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK VERSATILE PLATE 12 HOLES 3.5MM
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
GMReis Ankle Plating System ANATOMICAL MEDIAL TIBIA DISTAL VERSALOCK PLATE RIGHT 10 HOLES 2.7/3.5MM
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Cortical Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Scapular Medial Border Plate Right 06 Holes 3.5mm
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK LOCKING SCREW TI T7 Ø2.7X42.0MM
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis VA Screw
FDA UDI
Class IIActive
Orthopedic Instruments Ø1,5x31,0x62,0mm DRILL
FDA UDI
Class IActive
Mini and Micro Fragments Reconstruction System - GMReis PLATE
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Proximal Humerus Plate 03 Holes 3.5mm
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Proximal Femur Plate
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Cuboid Plate
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini L Plate
FDA UDI
Class IIActive
Pedimax II - Pedicular Screw Spinal System Rod
FDA UDI
Class IIActive
Orthopedic Instruments DRILL BIT DIAM.2.0 MM X 41.0 MM X 71.0 MM
FDA UDI
Class IActive
Mini and Micro Fragments Reconstruction System - GMReis VERSALOCK VOLAR BABY FOOT LOCKED PLATE E 56,0MM X 21,0MM
FDA UDI
Class IIUnknown
Versalock Periprosthetic Femur Plates System-GMReis Condilar Plate
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Micro Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini Cortical Screw
FDA UDI
Class IIActive
Versalock Upper Limb Plating System Versalock Hook Clavicle Plate Right 15.0mm 09 Holes 2.7/3.5mm
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK LOCKING SCREW TI T7 Ø2.7X56.0MM
FDA UDI
Class IIActive
EXPERT - Joint Fixation System EXPERT Knotless
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK TORXDRIVE LOCKING SCREW LOW PROFILE Ø3.5/2.7MM X70MM T10
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Locking Screw
FDA UDI
Class IIActive
Cut Screw - Percutaneous Compression Screw Cut Screw
FDA UDI
Class IIActive
Quick - Radius Disposable Set Quick - Radius Disposable Set - Small Plate Left and Screws
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Max Zip Anchor
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini Cortical Screw
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSA TORXDRIVE SCREW LOW PROFILE Ø3.5/2.7MMX46MM T10
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Locking Screw
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Locking Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis LOCKED VERSALOCK PLATE FLP EXTRA LONG 250,0MM – LEFT
FDA UDI
Class IIUnknown
GMReis Ankle Plating System VERSA TORXDRIVE SCREW LOW PROFILE Ø3.5/2.7MMX30MM T10
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis VERSALOCK VOLAR BABY FOOT LOCKED PLATE E 45,0MM X 21,0MM
FDA UDI
Class IIUnknown
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors Max Zip Anchor
FDA UDI
Class IIActive
GMReis Ankle Plating System VERSALOCK LOCKING SCREW TI T7 Ø2.7X6.0MM
FDA UDI
Class IIActive
Versalock Periprosthetic Femur Plates System-GMReis Cortical Screw
FDA UDI
Class IIActive
Mini and Micro Fragments Reconstruction System - GMReis Mini L Plate
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