Is this your brand? Sign in to claim ownership.
Sign in to claim this brandNeo Medical Inc.
US
Last updated September 17, 2026
What Neo Medical Inc. makes
Neo Medical Inc. makes a range of medical devices, including metallic spinal interbody fusion cages, spinal bone screws, and peripheral intravenous catheterization kits. They also produce vascular catheter introduction sets, nerve-locating anaesthesia needles, and general external orthopaedic fixation system implantation kits. Specific examples of their devices include the Neo Medical Cage kit, Neo Medical Pedicle screw kit, and V-Cath.
The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA 510(k) and FDA UDI registries. Neo Medical Inc. is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of products does Neo Medical Inc. manufacture?
Neo Medical Inc. makes medical devices like metallic spinal interbody fusion cages, spinal bone screws, and peripheral intravenous catheterization kits, because these are listed as their device categories.
Where is Neo Medical Inc. based?
Neo Medical Inc. is based in the US, as indicated by the country information provided.
Which registries list Neo Medical Inc.'s devices?
Neo Medical Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, because these are the registries mentioned in the device data.
How are Neo Medical Inc.'s devices classified?
Neo Medical Inc.'s devices are classified as Class I and Class II devices, because these are the device classes specified in the device data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 249 Freeport Blvd, Sparks, NV, 89431
- Website
- neomedicalinc.com
- —
- —
- [email protected]
- Phone
- 888-450-3334
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3007207906
- DUNS Number
- 015510540
Catalogue (302)
Page 7 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BonOs Inject Bone Cement; NEO Pedicle Screw System | K212489 | FDA 510(k) | Class II | Active |
| BonOs® Inject Bone Cement; NEO Pedicle Screw System™ | K222256 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
There is 1 recall record for Neo Medical Inc., initiated on 2011-04-05. The status of this recall is recorded as terminated. The reason given for the recall is that the firm received a recall notice from their contract manufacturer due to visible particulates in Bacteriostatic Sodium Chloride Injection, USP 0.9%, 30 mL vials that are included in insertion kits. This recall was both the earliest and most recent one initiated, as there is only one record.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 5, 2011 | Z-2223-2011 | — | terminated | Firm received recall notice from their contract manufacturer due to visible particulates in Bacteriostatic Sodium Chloride Injection, USP 0.9%, 30 mL vials that are included in insertion kits. |