Caliper, Ophthalmic
Ophthalmic · 21 CFR 886.4350
Recent MDR events
1 adverse event reports on file
Event type breakdown
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
162 firms currently registered for this product code
Aesculap, Inc.
CENTER VALLEY, PA, US
Instrumentarium Surgical Corp., Inc.
TERREBONNE Quebec, CA
Rumex International Co.
Tampa, FL, US
Sontec Instruments, Inc.
CENTENNIAL, CO, US
Kls Martin Se & Co. Kg
Muhlheim/Donau Baden-Wurttemberg, DE
Pilotis Tech Llc
Brookhaven, GA, US
Ambler Surgical, Llc
EXTON, PA, US
Dimeda Instrumente Gmbh
TUTTLINGEN Baden-Wurttemberg, DE
Phoenix Instruments, Inc.
Lisle, IL, US
Midwest Sterilization Corp.
JACKSON, MO, US
Surgix Medical Llc
Spring, TX, US
Microma Martin Alber Gmbh & Co. Kg
IRNDORF Baden-Wurttemberg, DE
Belle Healthcare Technology Co., Ltd.
Suzhou Jiangsu, CN
Indo-german Surgical Corporation
Mumbai Maharashtra, IN
Fischer Surgical Inc.
Imperial, MO, US
Iscon Surgicals, Ltd.
JODHPUR Rajasthan, IN
Aurora Surgical, Llc
St Petersburg, FL, US
Aesculap Ag
TUTTLINGEN, DONAU Baden-Wurttemberg, DE
Strub Medical Gmbh & Co. Kg
NEUHAUSEN Baden-Wurttemberg, DE
Med2b Ltd.
Kitzingen Bavaria, DE
Cambrian Medical, Inc.
Cedar City, UT, US
Sklar Corporation - Warehouse
Salisbury, MD, US
Kls Martin Se & Co. Kg
Fridingen Baden-Wurttemberg, DE
Teleflex Llc (nadc)
Olive Branch, MS, US
Synergy Health Sterilisation Uk Ltd
Thorne Doncaster, GB
510(k) clearances
7 clearances for this product code
- CooperVision, Inc.Apr 1, 1988
K881094 · KOI(TM) BLADE GAUGE, MODEL KOI-132
- Design Research Assoc., Inc.Mar 1, 1982
K813315 · CALIPER-OPTHALMIC
- Accutome, Inc.Feb 24, 1982
K820050 · KREMER BLADE GAUGE
- Koi, Inc.Jul 28, 1981
K812011 · BLADE GAUGE
- Aztec Medical Products, Inc.Sep 16, 1980
K801937 · BLEPHAROMETER
- V. Mueller O.V. Baxter Healthcare Corp.Dec 11, 1979
K792383 · KELMAN DIPSTICK
- Edward Weck, Inc.Dec 4, 1978
K781715 · RULER, WECK SCOTT