Identity
- Trade Name
- M-Brace Air FDA UDI
- Generic Name
- Lumbar spine orthosis FDA UDI
- Device Name
- This Lumblock Lumbar Back Brace acts as an immobilizing device for the lumbar-sacral region and its primary function is to reduce pain caused by lumbago, sciatica and ischialgia. Made with semi-rigid cotton fabric, it enjoys a structure made with eight self modeling and flexible steel stays on which a number of rigid straps slide. When the locking system is pulled and secured at the front, the inside straps stiffen the entire structure, thus effectively immobilizing the lumbar-sacral region. Practical and easy to wear, this Lumblock back brace perfectly adapts to whatever size and body type, thus ensuring maximum support and comfort at the desired tension. Through a new locking technology, operated by means of two crossing bands, the closing system is totally user friendly and allows a wide range of elastic tension settings. The Extra-Lumblock back brace model (#573) carry two additional sleeves at the back where custom moldable, anodized aluminum stays have been inserted. Although the rigidity of these braces has been remarkably increased, the comfort characteristics remain unaltered. INDICATIONS Disc complaints. Spondylo-arthrosis. Osteoporosis related lumbar vertebrae complaints. Para-vertebral lumbar muscle spasm. Light trauma of the lumbar-sacral column. Practical and easy to fit, it adapts perfectly to your body. This corset acts as a corrective measure and as a support to postural defects. Breathable and non allergenic, 100% cotton Back is 13” high Front is 8” high FDA UDI
- Model / Reference
- 573 XXL FDA UDI
- Description
- This Lumblock Lumbar Back Brace acts as an immobilizing device for the lumbar-sacral region and its primary function is to reduce pain caused by lumbago, sciatica and ischialgia. Made with semi-rigid cotton fabric, it enjoys a structure made with eight self modeling and flexible steel stays on which a number of rigid straps slide. When the locking system is pulled and secured at the front, the inside straps stiffen the entire structure, thus effectively immobilizing the lumbar-sacral region. Practical and easy to wear, this Lumblock back brace perfectly adapts to whatever size and body type, thus ensuring maximum support and comfort at the desired tension. Through a new locking technology, operated by means of two crossing bands, the closing system is totally user friendly and allows a wide range of elastic tension settings. The Extra-Lumblock back brace model (#573) carry two additional sleeves at the back where custom moldable, anodized aluminum stays have been inserted. Although the rigidity of these braces has been remarkably increased, the comfort characteristics remain unaltered. INDICATIONS Disc complaints. Spondylo-arthrosis. Osteoporosis related lumbar vertebrae complaints. Para-vertebral lumbar muscle spasm. Light trauma of the lumbar-sacral column. Practical and easy to fit, it adapts perfectly to your body. This corset acts as a corrective measure and as a support to postural defects. Breathable and non allergenic, 100% cotton Back is 13” high Front is 8” high FDA UDI
Identifiers
- Catalog Number
- 573 FDA UDI
- Primary DI / UDI-DI
- 05391512280789 FDA UDI
- FDA Product Code
- IQE FDA UDI
- GMDN Term
- Lumbar spine orthosis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3490 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Lumbar spine orthosis
M-Brace Air by Indaco Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Indaco Srl
Sources (1)
- FDA UDI e992747b-8ac9-4e3e-8989-9ee6a32a0b19 35 fields · synced May 30, 2026