Surgical Specialties Corporation Limited (UK)

FDA Device Registration & Listing · Taunton Somerset, GB · Registration 3007109793

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007109793
FEI Number
3007109793
Entity Name
Surgical Specialties Corporation Limited (UK)
City/State/Country
Taunton Somerset, GB
Establishment Address
Tancred Street, Taunton Somerset TA1 1RY, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Corza Medical Inc (Owner Number: 9060279)
Owner / Operator Contact Address
2755 Canyon Boulevard 1st Floor, Boulder, CO 80302, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tightrope Tightrope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
GAP Suture, Nonabsorbable, Silk General, Plastic Surgery Class 2 878.5030 2013-02-01
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2013-02-01
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2013-02-01
GAS Suture, Nonabsorbable, Synthetic, Polyester General, Plastic Surgery Class 2 878.5000 2013-02-01
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2024-06-07
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2013-02-01
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2024-06-07
MAI Fastener, Fixation, Biodegradable, Soft Tissue Orthopedic Class 2 888.3030 2024-06-07
LZB Finger Cot General Hospital Class 1 880.6250 2015-06-01
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2013-02-01
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2013-02-01
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2013-02-01
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2015-06-01
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2015-06-01

Official Correspondent

Alex Castillo

US Agent Details

Alex Castillo Email: RegulatoryAffairs@corza.com Phone: (619) 6178100

Related Public Records

Same Entity

Corza Medical Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011767135 SSC- Surgical Specialties Corporation Chula Vista, CA, US
3010692967 Surgical Specialties Mexico S DE RL DE CV Tijuana Baja California, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K072322 Smith & Nephew, Inc. ULTRA FAST-FIX AND ULTRA FAST-FIX AB MENISCAL REPAIR SYSTEMS 2007-09-18
K241486 Covidien Sofsilk™ Coated Braided Silk Suture 2024-12-03
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007109793. Last updated year: 2026. Please use registration number 3007109793 when referencing this establishment in official correspondence.
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