TechNH, INC.

FDA Device Registration & Listing · MERRIMACK, NH, US · Registration 1223651

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
1223651
FEI Number
1000159424
Entity Name
TechNH, INC.
City/State/Country
MERRIMACK, NH, US
Establishment Address
8 CONTINENTAL BLVD, MERRIMACK, NH 03054, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TECH, INC. (Owner Number: 9007626)
Owner / Operator Contact Address
8 CONTINENTAL BLVD., --, Merrimack, NH 03054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HV Heart Retractor MICROSPACER Spirette, EasyOne FlowTube

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWS Instruments, Surgical, Cardiovascular Cardiovascular Class 1 870.4500 2013-08-27
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2013-01-07
BYP Mouthpiece, Breathing Anesthesiology Class 1 868.5620 1993-05-12

Official Correspondent

Kevin Burnell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-04 Rultract Inc 1
Rultract Surgical Retractor, 4100 Series, all system configurations, reusable.
Z-0009-2007 Smith & Nephew Inc 1
Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007 Smith & Nephew Inc 1
Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06 Stryker Howmedica Osteonics Corp. 1
Allocraft TLIF Bone Inserter.
Z-0011-2007 Smith & Nephew Inc 1
Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1223651. Last updated year: 2026. Please use registration number 1223651 when referencing this establishment in official correspondence.
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