CoapTech, Inc.

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3015177732

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015177732
FEI Number
3015177732
Entity Name
CoapTech, Inc.
City/State/Country
Baltimore, MD, US
Establishment Address
101 W. Dickman Street, Suite 700, Baltimore, MD 21230, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device,Repack or Relabel Medical Device
Owner / Operator
CoapTech (Owner Number: 10058608)
Owner / Operator Contact Address
101 W Dickman St, Suite 700, Baltimore, MD 21230, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223916
PMA Number
N/A

All Registered Proprietary Names

PUMA-G Pediatric System PUMA-G System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGC Tube, Gastro-Enterostomy Gastroenterology, Urology Class 2 876.5980 2025-12-03
KGC Tube, Gastro-Enterostomy Gastroenterology, Urology Class 2 876.5980 2024-02-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CoapTech
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015177732. Last updated year: 2026. Please use registration number 3015177732 when referencing this establishment in official correspondence.
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