Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013164247

FEI Number

3013164247

Entity Name

CYPRESS ADAPTIVE, LLC

City/State/Country

Atlantic Highlands, NJ, US

Establishment Address

12 West Lincoln Ave., Unit D, Atlantic Highlands, NJ 07716, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Cypress Adaptive (Owner Number: 10052712)

Owner / Operator Contact Address

12 West Lincoln Ave, Unit D, P.O. Box 270, Navesink, New Jersey 07752, Atlantic Highlands, NJ 07716, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Actua Knee Vista Ankle Vista Ankle HY Paseo Knee Neoflex Active Neoflex Neoflex Junior

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISY	Joint, Knee, External Limb Component	Physical Medicine	Class 1	890.3420	2016-09-18
ISS	Prosthesis, Thigh Socket, External Component	Physical Medicine	Class 1	890.3420	2017-12-28

Official Correspondent

L Snyder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cypress Adaptive

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3005245962	TIMED INC.	Torrance, CA, US
3012035815	LEGWORKS	Buffalo, NY, US
1834241	College Park Industries	Warren, MI, US
8010401	STREIFENEDER ortho.production gmbH	EMMERING Bavaria, DE
1043533	U.S. ORTHOTICS, INC.	Tampa, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013164247. Last updated year: 2026. Please use registration number 3013164247 when referencing this establishment in official correspondence.