Camntech

Fenstanton Cambridgeshire, GB

CAMNTECH appears in FDA device records in Fenstanton Cambridgeshire, GB. FDA records list 2 510(k) clearances between 2010-04-29 and 2014-01-21, no PMA records and 2 registered establishments. As of 2026-09-10, FDA records show no recalls for this company, and at least one establishment registration is current.

510(k) clearances: 2
PMA records: 0
Recall records: 0
Registered establishments: 2

510(k) clearance history

FDA records hold 2 510(k) clearances for Camntech between 2010 and 2014. The busiest year on record is 2010, with 1. The most recent is 2014, with 1.

Clearances by year, as a table

510(k) clearance decisions for Camntech, by decision year
Year	Clearances
2010	1
2014	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K132764	MOTION WATCH AND PRO-DIARY	LEL	Substantially Equivalent	2014-01-21
K100266	ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603	MWJ	Substantially Equivalent	2010-04-29

Registered establishments

FDA registered establishments for Camntech, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3007485597	3007485597	CAMNTECH	Manor Farm, Fenstanton Cambridgeshire PE289JD GB	2026	GWK LEL
3008850182	3008850182	CAMNTECH, INC.	630 Boerne Stage Airfield, Boerne, TX 78006 US	2026	No device listings on this registration

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain