Identity
- Trade Name
- SalivaMAX FDA UDI
- Generic Name
- Artificial saliva FDA UDI
- Device Name
- SalivaMAX is a supersaturated calcium phosphate powder that when dissolved in water, creates a solution with a high concentration of electrolytes similar to that of natural saliva. SalivaMAX is an artificial saliva that is used to relieve acute and chronic symptoms of xerostomia and mucositis. FDA UDI
- Model / Reference
- SalivaMAX 30ct FDA UDI
- Description
- SalivaMAX is a supersaturated calcium phosphate powder that when dissolved in water, creates a solution with a high concentration of electrolytes similar to that of natural saliva. SalivaMAX is an artificial saliva that is used to relieve acute and chronic symptoms of xerostomia and mucositis. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00370275629030 FDA UDI
- 510(k) Number
- K152406 FDA UDI
- FDA Product Code
- LFD FDA UDI
- GMDN Term
- Artificial saliva FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Artificial saliva
SalivaMAX by Forward Science Technologies Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Artificial saliva.
- THERABREATH RINSE — Church & Dwight Co., Inc. · U
- Biotene — Haleon US Holdings LLC · U
- Biotene — Haleon US Holdings LLC · U
- Moisyn Dry Mouth Oral Mist — Synedgen, Inc. · U
- Salivea — Laclede, Inc. · U
- Biotene Oral Rinse Dry Mouth — Haleon US Holdings LLC · U
- THERABREATH LOZENGE — Church & Dwight Co., Inc. · U
- Periovance Dry Mouth Gel — ORABIO, INC. · U
Cleared under the same submission
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 U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Forward Science Technologies Llc
Sources (1)
- FDA UDI 7b1ff7d4-3640-40ab-8808-5c58e0b776be 35 fields · synced Jun 8, 2026