PUTNAM MEDICAL CORP.

FDA Device Registration & Listing · Dayville, CT, US · Registration 3017059666

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
3017059666
FEI Number
3017059666
Entity Name
PUTNAM MEDICAL CORP.
City/State/Country
Dayville, CT, US
Establishment Address
329 Lake Rd, Dayville, CT 06241, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Putnam Medical Corporation (Owner Number: 10075923)
Owner / Operator Contact Address
329 Lake Rd, Dayville, CT 06241, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Standard Bariatrics Standard Bougie SB38 Standard Precision Bougie Device; Standard Tapered Bougie, 38 Fr (STB38)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2021-07-10
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2022-05-25
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2022-12-02

Official Correspondent

Holly Opalenik

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K900590 Biosearch Medical Products, Inc. BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING 1990-08-02
K102548 Footprint Medical, Inc. FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE 2010-11-26
K955248 United States Endoscopy Group, Inc. U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT 1996-05-21
K872921 Medical Support, Inc. MSS ENTERAL DELIVERY SET 1987-12-03
K180622 Covidien Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port 2018-10-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-2022 Medtronic Perfusion Systems 2
Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
Z-0021-2018 OriGen Biomedical, Inc. 2
The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.

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3009247326 Jabil Circuit (Singapore) Pte Ltd Singapore Central Singapore, SG
2528981 LYNX Medical Pennsylvania ERIE, PA, US
1649518 Sterigenics US LLC Fort Worth, TX, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017059666. Last updated year: 2026. Please use registration number 3017059666 when referencing this establishment in official correspondence.
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