FDA.reportPublic FDA data

Reflux Band

Primary DI
00866736000307
Brand
Reflux Band
Company
The Reflux Company
Model
101-1170-00
Device description
External upper-esophageal sphincter compression device.
Published
2026-10-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
PKAExternal Upper Esophageal Sphincter (Ues) Compression Device

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
PKAExternal Upper Esophageal Sphincter (Ues) Compression DeviceEar, Nose, Throat2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K173934000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K173934000Reza Band, Reflux BandSomna Therapeutics, LLC2018-04-13PKA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00866736000307PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00866736000307008667360003078667360003070866736000307

GMDN Terms#

Term, Definition table
TermDefinition
Gastro-oesophageal antireflux barrierAn orally-administered substance intended to protect the gastro-oesophageal mucosa from gastric acid reflux through formation of a barrier plug following ingestion. It typically contains a gel-forming substance (e.g., alginate) that swells to form a plug near the gastro-oesophageal junction after contact with stomach acids, thereby physically preventing the reflux; the plug subsequently biodegrades for gastrointestinal elimination. The device is normally available in the form of a tablet or gel for home-use, and may be used to treat gastro-oesophageal reflux disease (GERD) of various causes. This is a single-use device.

Contacts#

Phone, Email table
PhoneEmail
858-397-2200contact@refluxcompany.com

Regulatory Flags#

DUNS number
144845049
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00866736000314Reflux Band Manometer101-250-002026-10-08
00866736000383Reflux Band Pressure Sensor101-1290-002026-10-08
00899994002097RestechDx-201 pH probe CAS2022-12-02
00899994002103RestechDx-10002022-12-02
00899994002110RestechDx-3002022-12-02
00899994002127RestechDx-5002022-12-02
00899994002134RestechDx-201 P2022-12-02
00899994002141RestechDx-201 L 2022-12-02
00856219002102Mederi MDRF1 GeneratorMDRF1177-51502016-09-27
00856219002294Stretta8800175-55802016-09-27
00856219002003Secca8000175-51072016-09-27

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10197106827376CARDINAL HEALTHCardinal Health 200, LLCPKA2024-12-18
50197106827374CARDINAL HEALTHCardinal Health 200, LLCPKA2024-12-18
10197106743171CARDINAL HEALTHCardinal Health 200, LLCPKA2024-09-26
50197106743179CARDINAL HEALTHCardinal Health 200, LLCPKA2024-09-26
10197106690437CARDINAL HEALTHCardinal Health 200, LLCPKA2024-07-16
50197106690435CARDINAL HEALTHCardinal Health 200, LLCPKA2024-07-16
10197106652015CARDINAL HEALTHCardinal Health 200, LLCPKA2024-06-15
50197106652013CARDINAL HEALTHCardinal Health 200, LLCPKA2024-06-15
10197106655030CARDINAL HEALTHCardinal Health 200, LLCPKA2024-05-16
50197106655038CARDINAL HEALTHCardinal Health 200, LLCPKA2024-05-16
10197106626474CARDINAL HEALTHCardinal Health 200, LLCPKA2024-04-26
50197106626472CARDINAL HEALTHCardinal Health 200, LLCPKA2024-04-26
10197106524589CARDINAL HEALTHCardinal Health 200, LLCPKA2024-02-29
50197106524587CARDINAL HEALTHCardinal Health 200, LLCPKA2024-02-29
10197106572887CARDINAL HEALTHCardinal Health 200, LLCPKA2024-02-12
50197106572885CARDINAL HEALTHCardinal Health 200, LLCPKA2024-02-12
10197106481875CARDINAL HEALTHCardinal Health 200, LLCPKA2023-12-27
50197106481873CARDINAL HEALTHCardinal Health 200, LLCPKA2023-12-27
10197106293171CARDINAL HEALTHCardinal Health 200, LLCPKA2023-06-23
50197106293179CARDINAL HEALTHCardinal Health 200, LLCPKA2023-06-23
10197106295083CARDINAL HEALTHCardinal Health 200, LLCPKA2023-06-14
50197106295081CARDINAL HEALTHCardinal Health 200, LLCPKA2023-06-14
10197106210567CARDINAL HEALTHCardinal Health 200, LLCPKA2023-05-04
50197106210565CARDINAL HEALTHCardinal Health 200, LLCPKA2023-05-04
10197106191491CARDINAL HEALTHCardinal Health 200, LLCPKA2023-03-29
50197106191499CARDINAL HEALTHCardinal Health 200, LLCPKA2023-03-29