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Sign in to claim this brandORTHO ARCH COMPANY INC
US
Last updated September 17, 2026
What ORTHO ARCH COMPANY INC makes
Ortho Arch Company Inc manufactures orthodontic devices including archwires (such as Super Elastic Nickel Titanium and Stainless Steel Goldtone varieties), metal and ceramic brackets (including self-ligating types like Solo Twin and Eclipse Interactive), molar bands (such as Conlin and HalO), inter-arch elastic bands, and orthodontic pliers. Specific product examples include Accu Twin, Eclipse Passive, Regular Glide-Ties, and various nickel titanium and stainless steel archwires.
The company's devices are classified as FDA Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) system. Ortho Arch Company Inc is based in 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 orthodontic devices does Ortho Arch Company Inc manufacture?
Ortho Arch Company Inc manufactures orthodontic archwires (including Super Elastic Nickel Titanium and Stainless Steel Goldtone varieties), metal and ceramic brackets (such as self-ligating Solo Twin and Eclipse Interactive types), molar bands (like Conlin and HalO), inter-arch elastic bands, and orthodontic pliers. These products are explicitly listed in the device data as the company's core offerings, with examples including Accu Twin, Eclipse Passive, Regular Glide-Ties, and various archwire types.
Where is Ortho Arch Company Inc based?
Ortho Arch Company Inc is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field confirms this as US, indicating the company's headquarters or primary operational location is within the United States.
In which regulatory registry are Ortho Arch Company Inc's devices listed?
Ortho Arch Company Inc's devices are listed in the FDA's Unique Device Identification (fda_udi) system, as specified in the LISTED IN field of the device data. This registry tracks medical devices sold in the United States and requires manufacturers to submit device identifiers for traceability and post-market surveillance.
How are Ortho Arch Company Inc's devices classified by regulatory authorities?
Ortho Arch Company Inc's devices are classified as FDA Class I and Class II medical devices, as stated in the DEVICE CLASSES field and reiterated in the SUMMARY. This classification reflects the level of regulatory control required, with Class I devices subject to general controls and Class II devices requiring additional special controls such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 1107 Tower Road, Schaumburg, IL, 60173
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3007284437
- DUNS Number
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Catalogue (3144)
Page 41 of 63| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Horizon Mini Twin Bracket | .022 LBICL 12T | FDA UDI | Class I | Active |
| Conlin Molar Band | LR 34.5 MOLAR BAND | FDA UDI | Class I | Active |
| Lip Bumper | 271-340 | FDA UDI | Class I | Active |
| Nova-S-Sapphire Bracket | .018 U3L HK ROTH | FDA UDI | Class II | Active |
| Spectrum | MINI LIGATURE CUTTER | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket | .018 LBIC -17T | FDA UDI | Class I | Active |
| Razor | 800-230 | FDA UDI | Class I | Active |
| Regular Glide-Ties | 300-203 | FDA UDI | Class I | Active |
| Mini Glide-Ties | 300-122 | FDA UDI | Class I | Active |
| Conlin Molar Bands | UR3 MB W/036 LW BT & LC 32 | FDA UDI | Class I | Active |
| Super Elastic Nickel Titanium Archwire | 226-013 | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket | .022 UBICR ROTH | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket | .022 U1L +22T | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket System | .018 ROTH HIGH TORQUE | FDA UDI | Class I | Active |
| Constant Force Nickel Titanium Spring | 226-293 | FDA UDI | Class I | Active |
| Roth Mini Plus | 0.18 LL3 W/HK | FDA UDI | Class I | Active |
| Accu Twin Bracket | 462-362 | FDA UDI | Class I | Active |
| Super Elastic Nickel Titanium Archwire | 226-001G | FDA UDI | Class I | Active |
| Spectrum | 800-130 | FDA UDI | Class I | Active |
| Spectrum | ADHESIVE REMOVER | FDA UDI | Class I | Active |
| Micro Twin Bracket | 464-411 | FDA UDI | Class I | Active |
| Beta Titanium Archwire | 228-730M | FDA UDI | Class I | Active |
| Accu Twin Bracket | 462-171 | FDA UDI | Class I | Active |
| Beta-T | .016X.022 MUSHROOM LOOP 26MM | FDA UDI | Class I | Active |
| Clear-Lock Ceramic | 466-862 | FDA UDI | Class II | Active |
| Micro Twin Bracket | 464-671 | FDA UDI | Class I | Active |
| Spectrum | V-BEND STOP | FDA UDI | Class I | Active |
| Elastomeric Thread | 340-130 | FDA UDI | Class I | Active |
| Halo Molar Band | U6L MOLAR BAND .022 0T BT W/SHEATH | FDA UDI | Class I | Active |
| Solo Twin Bracket | 462-762 | FDA UDI | Class I | Active |
| Intraoral Elastics | 360-504 | FDA UDI | Class I | Active |
| Conlin Molar Band | MOLAR BAND RX UR3 7 | FDA UDI | Class I | Active |
| Conlin Molar Band | LR 31 MOLAR BAND | FDA UDI | Class I | Active |
| Conlin Molar Band | LR 30 MOLAR BAND | FDA UDI | Class I | Active |
| Preformed Ligature Wire | 270-018 | FDA UDI | Class I | Active |
| Conlin Molar Band | LR 29.5 MOLAR BAND | FDA UDI | Class I | Active |
| Intraoral Elastics | 350-324 | FDA UDI | Class I | Active |
| Super Elastic Nickel Titanium Archwire | 226-4130G | FDA UDI | Class I | Active |
| Conlin Molar Bands | LL MB W/036 LW BT & LC 43 | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket | .022 U1L MBT | FDA UDI | Class I | Active |
| Ligature Ties | 270-016 | FDA UDI | Class I | Active |
| Stainless Steel Archwire | 250-171 | FDA UDI | Class I | Active |
| Horizon Mini Twin Bracket | .018 LBICR 12T | FDA UDI | Class I | Active |
| Mini Glide-Ties | 300-116 | FDA UDI | Class I | Active |
| Super Elastic Nickel Titanium Archwire | 226-0000G | FDA UDI | Class I | Active |
| Accu Twin Bracket | 462-252 | FDA UDI | Class I | Active |
| Eclipse Interactive | 461-671 | FDA UDI | Class I | Active |
| heat activated nitinol archwire | 226-515 | FDA UDI | Class I | Active |
| Tissue Guard | 340-309 | FDA UDI | Class I | Active |
| Nova C Ceramic | 464-901 | FDA UDI | Class II | Active |
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