HomeUSAPeregrine Surgical , Ltd.

Peregrine Surgical , Ltd.

USA · New Britain
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Taiwan, South Korea, Australia — 6 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
11listed device types
Class I 5Class II 6Class III 0
plus 25 registration records and 20 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
5registered devices
Class I 1Class II 4
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
3 including historic records
TWTaiwanTFDA
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
3GMP quality-system certificates
Import 3
AUAustraliaTGA ARTG
3active ARTG entries
IIa 3
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States25 registration records, 20 510(k), 0 PMA
Brazil5 confirmed, 0 excluded
Manufacturer names merged into this page: Peregrine Surgical, LLC. · PEREGRINE SURGICAL, LLC · PEREGRINE SURGICAL LTD. · PEREGRINE SURGICAL LLC.

Company information

Country
USA
City
New Britain

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

31994
11995
71998
11999
22003
12006
32013
12015
12024

FDA listed device types

showing 8 of 11
Instrument, Vitreous Aspiration And Cutting, Ac-Powered 1Laser, Ophthalmic 1Photocoagulator And Accessories 1Endoilluminator 1Unit, Phacofragmentation 1Powered Laser Surgical Instrument 1Ring, Ophthalmic (Flieringa) 1Cannula, Ophthalmic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK233653Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)2024-08-05
USK15160423ga Chandelier Illuminator, 25ga Chandelier Illuminator2015-09-11
USK132614PEREGRINE CURVED ILLUMINATING LASER PROBE2013-11-14
BR80122640027CANULAS DE RETINAClass II
BR80122640025PINÇAS DE RETINA DESCARTÁVEISClass II
BR80686670003ILM FORCEPSClass I

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