Medical Device Manufacturer · DE , Kaufbeuren

NOUVAG AG - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1996

Recent clearances: LipoSurg ARTIST, MORCE POWER PLUS AND VARIOCARVE MORCELLATOR, TCM ENDO 20

View 12 510(k) Devices ↓

Total

Cleared

Denied

NOUVAG AG has 12 FDA 510(k) cleared medical devices. Based in Kaufbeuren, DE.

Latest FDA clearance: Sep 2026. Active since 1996. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by NOUVAG AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Ken Block Consulting, LLC as regulatory consultant.

NOUVAG AG is one of 502 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - NOUVAG AG

12 devices

1-12 of 12

Cleared Sep 05, 2026

LipoSurg ARTIST

K254135 · QPB

General & Plastic Surgery · 257d

Cleared Jun 29, 2009

MORCE POWER PLUS AND VARIOCARVE MORCELLATOR

K080365 · HET

Obstetrics & Gynecology · 504d

General Hospital · 168d

Cleared Dec 22, 2004

TCM ENDO V, MODEL 1534

K042822 · EKX

Dental · 71d

Cleared Dec 17, 2004

NOUVAG AG - VACUSON 40 AND VACUSON 60

K042943 · BTA

General & Plastic Surgery · 53d

Cleared Nov 03, 2004

MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55

K042434 · DZI

Dental · 56d

Cleared Oct 01, 2003

CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061,...

MD 10, SEM, SM 12, CBM

K000710 · EFB

Dental · 70d

Cleared Feb 09, 1999

TCM 3000 AND TCM ENDO

K981679 · EFB

Dental · 272d

Cleared Jan 16, 1996

MICRO-DISPENSER 7000 & MICRODISPENSER 8000

K954722 · EFB

Dental · 95d

NOUVAG AG - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - NOUVAG AG

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