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Back-n-Shape II

FDA UDI

Class I (US FDA UDI)

by Medical Specialties Incorporated

Identity

Trade Name
Back-n-Shape II FDA UDI
Generic Name
Lumbar spine orthosis FDA UDI
Model / Reference
163035 FDA UDI

Identifiers

Primary DI / UDI-DI
00802357630356 FDA UDI
FDA Product Code
IPY 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

No

FDA UDI

Over-the-Counter

No

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

Back-n-Shape II by Medical Specialties Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumbar spine orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb33032d-8d4c-4116-96f8-4b91f70f8d49 32 fields · synced Jun 8, 2026